Molecular analysis of chromosome region 11p13 in patients with Drash syndrome (Q34592296)

3 August 2017

Molecular analysis of chromosome region 11p13 in patients with Drash syndrome (English)

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3 August 2017

Jadresic L

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Wadey RB

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Buckle B

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Barratt TM

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Mitchell CD

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Cowell JK

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language of work or name

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1 March 1991

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497-501

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https://scigraph.springernature.com/pub.10.1007/bf00194641

3 August 2017

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cites work

The association of Wilms' tumor, male pseudohermaphroditism and diffuse glomerular disease (Drash syndrome): report of eight cases with clinical and morphologic findings and review of the literature

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12 December 2020

Pseudohermaphroditism, glomerulopathy, and Wilms tumor (Drash syndrome)

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12 December 2020

Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.

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12 December 2020

Predisposition to retinoblastoma due to a translocation within the 4.7R locus

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12 December 2020

Epidemiological features of Wilms' tumor: results of the National Wilms' Tumor Study

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12 December 2020

Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome).

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12 December 2020

The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.

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12 December 2020

ASSOCIATION OF NEPHROTIC SYNDROME AND NEPHROBLASTOMA IN SIBLINGS

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12 December 2020

The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): a distinctive glomerular lesion--report of 10 cases

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12 December 2020

Complete and incomplete Drash syndrome: a clinicopathologic study of five cases of a dysontogenetic-neoplastic complex.

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12 December 2020

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

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12 December 2020

Genetic evidence that ZFY is not the testis-determining factor

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12 December 2020

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

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12 December 2020

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

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12 December 2020

Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome

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12 December 2020

A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

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12 December 2020

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells

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12 December 2020

Consistent chromosome abnormalities associated with mouse bladder epithelial cell lines transformed in vitro

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12 December 2020

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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12 December 2020

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

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12 December 2020

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

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12 December 2020

Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.

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12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

NEPHROBLASTOMA IN A CASE OF AGONADISM

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12 December 2020

Tumor suppressor genes: the puzzle and the promise

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12 December 2020

The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus

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12 December 2020

Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)].

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12 December 2020

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

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12 December 2020

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

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12 December 2020

Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism

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12 December 2020

Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.

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12 December 2020

Pseudohermaphroditism, glomerulopathy, and Wilms tumor (Drash syndrome): frequency in end-stage renal failure

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12 December 2020

Wilm's tumour, hypospadias, and cryptorchidism in twins

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12 December 2020

Bilateral renal agenesis

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12 December 2020

Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion

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12 December 2020

GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

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12 December 2020

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

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12 December 2020

Identifiers

DOI

10.1007/BF00194641

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Dimensions Publication ID

3 August 2017

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