(Q40282480)

19 September 2017

title

Aniridia Caused by a Heritable Chromosome 11 Deletion (English)

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35425-2

5 June 2022

1 reference

human chromosomes 6-12 and X

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A230439

chromosomal deletion syndrome

5 June 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A230439

5 June 2022

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35425-2

5 June 2022

author name string

H. M. Hittner

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A230439

5 June 2022

V. M. Riccardi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A230439

5 June 2022

U. Francke

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A230439

5 June 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=230439

5 June 2022

publication date

1 June 1979

1 reference

full work available at URL

19 September 2017

https://api.elsevier.com/content/article/PII:S0161642079354252?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35425-2

https://api.elsevier.com/content/article/PII:S0161642079354252?httpAccept=text/plain

5 June 2022

1 reference

https://api.crossref.org/works/10.1016/S0161-6420(79)35425-2

5 June 2022

1 reference

19 September 2017

volume

86

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19 September 2017

issue

6

1 reference

19 September 2017

page(s)

1173-1183

1 reference

Gene dose effect: intraband mapping of the <i>LDH A </i>locus using cells from four individuals with different interstitial deletions of 11p

19 September 2017

cites work

A familial syndrome of aniridia and absence of the patella

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Familial aniridia with preserved ocular function

19 January 2023

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ANIRIDIA, CEREBELLAR ATAXIA, AND OLIGOPHRENIA IN SIBLINGS.

19 January 2023

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Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia-Wilms' tumor syndrome

19 January 2023

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Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome II. A clinicopathological case report

19 January 2023

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ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS

19 January 2023

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The association of aniridia, Wilms's tumor, and genital abnormalities

19 January 2023

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WILMS'S TUMOR AND ASSOCIATED ANOMALIES

19 January 2023

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Relation between Cancer and Congenital Defects in Man

19 January 2023

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Aniridia and wilms's tumour (nephroblastoma)

19 January 2023

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Nephroblastoma (Wilms tumor) and congenital aniridia

19 January 2023

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Sporadic aniridia and Wilms' tumor.

19 January 2023

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Childhood cancer and congenital defects. A study of U.S. death certificates during the period 1960-1966.

19 January 2023

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Wilm's tumor with aniridia

19 January 2023

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Natural history and treatment of Wilms's tumour: an analysis of 335 cases occurring in England and Wales 1962-6.

19 January 2023

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Simultaneous occurrence of congenital aniridia, hamartoma, and Wilms' tumor

19 January 2023

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The association of congenital malformations and malignant tumors in infants and children

19 January 2023

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Wilm's-aniridia syndrome with transient hypo-gamma-globulinaemia of infancy

19 January 2023

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Wilms' tumor in seven children withcongenital aniridia

19 January 2023

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Congenital anomalies in children with Wilms' Tumor. A new survey

19 January 2023

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Wilms' tumor: Natural history and prognostic factors.A retrospective study of 248 cases treated at the institut Gustave-Roussy 1952–1967

19 January 2023

42

1 reference

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Aniridia-Wilms’ Tumour Syndrome

19 January 2023

45

1 reference

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Wilm's tumor coexisting with congenital bilateral absence of iris

19 January 2023

46

1 reference

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Aniridia, Cataracts, and wilms' Tumor in Monozygous Twins

19 January 2023

47

1 reference

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Chromosomal deletion and retinoblastoma

19 January 2023

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Mutation and cancer: a model for Wilms' tumor of the kidney

19 January 2023

49

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Mutation and cancer: statistical study of retinoblastoma

19 January 2023

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Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas

19 January 2023

52

1 reference

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19 January 2023

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=230439

19 January 2023

1 reference