(Q24674814)

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Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

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Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3 (English)

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author name string

N M Solomon

1

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S A Ross

2

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T Morgan

3

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J L Belsky

4

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F A Hol

5

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P S Karnes

6

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N J Hopwood

7

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S E Myers

8

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A S Tan

9

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G L Warne

10

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S M Forrest

11

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P Q Thomas

12

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language of work or name

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publication date

September 2004

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Journal of Medical Genetics

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41

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9

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669-78

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Sox3 Is Required for Gonadal Function, but Not Sex Determination, in Males and Females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

SOX3 is required during the formation of the hypothalamo-pituitary axis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

Signaling and transcriptional mechanisms in pituitary development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

Integrated FGF and BMP signaling controls the progression of progenitor cell differentiation and the emergence of pattern in the embryonic anterior pituitary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

Mouse Dll3: a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

Gsh-1, an orphan Hox gene, is required for normal pituitary development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

SOX3 is an X-linked gene related to SRY

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

7 April 2017

Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

Assembly of microarrays for genome-wide measurement of DNA copy number

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

Molecular basis of pituitary dysfunction in mouse and human.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

The molecular basis for developmental disorders of the pituitary gland in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

Tissue interactions in the induction of anterior pituitary: role of the ventral diencephalon, mesenchyme, and notochord

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

Variable X-linked recessive hypopituitarism with evidence of gonadotropin deficiency in two pre-pubertal males

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 September 2017

Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

30 May 2018

Effect of the basal diencephalon on the development of Rathke's pouch in rats: a study in combined organ cultures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

30 May 2018

Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 November 2018

A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 November 2018

Comparative expression of the mouse Sox1, Sox2 and Sox3 genes from pre-gastrulation to early somite stages.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 November 2018

Utah Growth Study: growth standards and the prevalence of growth hormone deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 November 2018

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735898

28 November 2018

Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

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The molecular genetics of growth hormone deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

based on heuristic

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Genome wide detection of oncogene amplifications in nasopharyngeal carcinoma by array based comparative genomic hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked congenital panhypopituitarism

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked recessive hypopituitarism

1 reference

https://pubmed.ncbi.nlm.nih.gov/15342697

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2003.016949

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