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Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization

author

Veronica van Heyningen

1946 -

published in: American Journal of Human Genetics

date of publication: 1992-12-01

language: English

Cites articles 40

Date

Title

Authors

1992-01-01

Wilms' tumour: reconciling genetics and biology

Veronica van Heyningen
1992-02-01

High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered

Rosalind John, Veronica van Heyningen, David J. Porteous
1991-10-01

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization

William B. Dobyns
1991-12-20

Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region

Veronica van Heyningen, Anand Swaroop
1991-12

Mouse small eye results from mutations in a paired-like homeobox-containing gene
1991-10-01

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
1991-10-01

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour.
1991-03-01

Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare

Annemarie Poustka
1991-10-01

The distal region of 11p13 and associated genetic diseases

Bryan R Williams, Veronica van Heyningen
1990-01-05

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones
1990-11-01

A mouse model of the aniridia-Wilms tumor deletion syndrome
1990-07-01

The candidate Wilms' tumour gene is involved in genitourinary development
1990-02-22

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

Manfred Gessler
1990-02-09

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
1990-06-21

Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
1990-07-01

Role for the Wilms tumor gene in genital development?

Veronica van Heyningen
1990-07-01

Parental origin of de novo constitutional deletions of chromosomal band 11p13
1990-10-01

Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus
1989-11-01

CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia

Veronica van Heyningen
1989-06-01

Cloning of breakpoints of a chromosome translocation identifies the AN2 locus.

Manfred Gessler
1989-04-01

A deletion map of the WAGR region on chromosome 11.
1988-11-01

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
1988-12-01

Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11.
1988-03-01

Age distribution of Wilms' tumor: report from the National Wilms' Tumor Study
1988-01-01

Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids

Veronica van Heyningen
1988-01-01

Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers

Veronica van Heyningen, David J. Porteous
1988-08-01

Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci
1988-01-01

Heritable fraction of unilateral Wilms tumor
1988-11-01

Lack of linkage of familial Wilms' tumour to chromosomal band 11p13
1988-07-01

Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumor

Joonsoo Kang
1987-08-01

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
1987-12-01

Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization

Article - wd:Q35196255

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