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Chromosomal abnormalities and mental illness.
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Europe PubMed Central
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12660800
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12660800%20AND%20SRC:MED&resulttype=core&format=json
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2 November 2019
review article
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title
Chromosomal abnormalities and mental illness
(English)
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Europe PubMed Central
PubMed publication ID
12660800
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2 November 2019
author
Donald J. MacIntyre
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12660800
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2 November 2019
David J. Porteous
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12660800
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2 November 2019
Benjamin S Pickard
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PubMed publication ID
12660800
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2 November 2019
Douglas Blackwood
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Blackwood DH
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12660800
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2 November 2019
Walter J Muir
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Muir WJ
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PubMed publication ID
12660800
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2 November 2019
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English
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1 March 2003
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Europe PubMed Central
PubMed publication ID
12660800
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2 November 2019
published in
Molecular Psychiatry
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PubMed publication ID
12660800
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2 November 2019
volume
8
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PubMed publication ID
12660800
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2 November 2019
issue
3
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12660800
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2 November 2019
page(s)
275-287
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Europe PubMed Central
PubMed publication ID
12660800
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retrieved
2 November 2019
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Susceptibility loci for bipolar disorder: overlap with inherited vulnerability to schizophrenia
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Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.
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Positional cloning: let's not call it reverse anymore
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‘Pfropfschizophrenie’ revisited
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Correlations between clinical and historical variables, and cerebral structural variables in people with mild intellectual disability and schizophrenia
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Association within a family of a balanced autosomal translocation with major mental illness
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Disruption of two novel genes by a translocation co-segregating with schizophrenia
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Chromosome 1 loci in Finnish schizophrenia families
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A Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic Disorders
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Chromosomal abnormalities and schizophrenia
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Chromosomal aberrations and bipolar affective disorder
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Schizophrenia and sex chromosome anomalies
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Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22
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A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
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A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.
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Partial trisomy chromosome 5 cosegregating with schizophrenia
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No evidence for linkage between chromosome 5 markers and schizophrenia
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Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1.
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Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis
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Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families
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Brief report: translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia
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Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
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inferred from DOI database lookup
Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mental disorder and inversion on chromosome 9
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome aberrations in patients with paranoid psychosis
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic findings in 250 schizophrenics: evidence confirming an excess of the X chromosome aneuploidies and pericentric inversion of chromosome 9
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Karyotype analysis of 161 unrelated schizophrenics: no increased rates of X chromosome mosaicism or inv(9), using ethnically matched and age-stratified controls
1 reference
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Paracentric inversion of chromosome 9 with schizoaffective disorder
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Schizophrenia and mental retardation in an adult male with a de novo interstitial deletion 9(q32q34.1)
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families
1 reference
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A schizophrenia locus may be located in region 10p15-p11.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
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7 January 2021
based on heuristic
inferred from DOI database lookup
Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
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7 January 2021
based on heuristic
inferred from DOI database lookup
A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
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7 January 2021
based on heuristic
inferred from DOI database lookup
Further investigation of a chromosome 15 locus in schizophrenia: Analysis of affected sibpairs from the NIMH genetics initiative
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
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7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence for linkage between schizophrenia and markers at chromosome 15q13-14.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence for linkage of the CHRNA7 gene region in Canadian schizophrenia families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic abnormalities on chromosome 18 associated with bipolar affective disorder or schizophrenia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A linkage study of bipolar illness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Affective disorder associated with a balanced translocation involving chromosome 14 and 18
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: a linkage study in 13 target chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of bipolar affective disorder to chromosome 18 markers in a new pedigree series.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential rates of psychiatric disorders in adults with Down's syndrome compared with other mentally handicapped adults
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial manic-depressive illness with deleted short arm of chromosome 21: coincidental or causal?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nonparametric simulation-based statistical analyses for bipolar affective disorder locus on chromosome 21q22.3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
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7 January 2021
based on heuristic
inferred from DOI database lookup
Late‐Onset psychosis in the velo‐cardio‐facial syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High rates of schizophrenia in adults with velo-cardio-facial syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide search for schizophrenia susceptibility genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Schizophrenia spectrum disorders: an autosomal-wide scan in multiplex pedigrees
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No evidence of increased risk for schizophrenia or bipolar affective disorder in persons with aneuploidies of the sex chromosomes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The clinical significance of fragile sites on human chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chemical differentiation along metaphase chromosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Initial sequencing and analysis of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High-resolution haplotype structure in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Integration of cytogenetic landmarks into the draft sequence of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Enhanced long-term potentiation and impaired learning in mice with mutant postsynaptic density-95 protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type I bipolar disorder associated with a fragile site on chromosome 1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trisomy 2q11.2-->q21.1 resulting from an unbalanced insertion in two generations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new heritable fragile site on human chromosome 3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of schizophrenia and partial trisomy of chromosome 5p. A case report
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A balanced chromosomal translocation partially co-segregating with psychotic illness in a family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome survey of new patients admitted to the four maximum security hospitals in the United Kingdom
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A cytogenetic study of children with psychiatric disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
D-D translocations in patients with mental illness.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prader-Willi syndrome and psychoses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 18 translocation (18;21) (p11.1;p11.1) associated with psychosis in one family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile 19p13 in a family with mental illness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mania and Down's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Major depression in a small group of adults with Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bipolar disorder associated with Turner's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The association between triple X and psychosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of Turner syndrome with schizophrenia: genetic relationship between Turner syndrome and psychosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Investigation of Turner syndrome in schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
XYY chromosome anomaly and schizophrenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Organic schizophrenic syndrome associated with symmetrical basal ganglia sclerosis and XO/XY-mosaic
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.MP.4001232
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/SJ.MP.4001232
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12660800
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12660800%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
PubMed publication ID
12660800
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12660800
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12660800%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
ResearchGate publication ID
10834595
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