Wilms's tumour and aniridia: clinical and cytogenetic features - Wikidata - awgldk - TriplyDB

Wilms's tumour and aniridia: clinical and cytogenetic features

Wilms's tumour and aniridia: clinical and cytogenetic features

http://www.wikidata.org/entity/Q35116296

about

Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders 11p13 deletion, Wilms' tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases.HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.A deletion map of the WAGR region on chromosome 11.Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.Sp1 is a critical regulator of the Wilms' tumor-1 gene.WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2).Perinatal (congenital and neonatal) neoplasms: a report of 110 cases.

P2860

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P2860

Wilms's tumour and aniridia: clinical and cytogenetic features

http://www.wikidata.org/entity/Q35116296

description

1982 nî lūn-bûn

@nan

1982 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

1982 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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1982年の論文

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1982年論文

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1982年論文

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1982年論文

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1982年論文

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1982年論文

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1982年论文

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name

Wilms's tumour and aniridia: clinical and cytogenetic features

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Wilms's tumour and aniridia: clinical and cytogenetic features

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type

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Wilms's tumour and aniridia: clinical and cytogenetic features

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Wilms's tumour and aniridia: clinical and cytogenetic features

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prefLabel

Wilms's tumour and aniridia: clinical and cytogenetic features

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Wilms's tumour and aniridia: clinical and cytogenetic features

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Archives of Disease in Childhood

P1476

Wilms's tumour and aniridia: clinical and cytogenetic features

@en

P2093

Harnden DG

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Harper E

http://www.w3.org/2001/XMLSchema#string

Herbert A

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Mann JR

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Morten JE

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Shannon RS

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P2860

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

The characterization of high-resolution G-banded chromosomes of man.

Assignment of three human genes to chromosomes (LDH-A to 11, TK to 17, and IDH to 20) and evidence for translocation between human and mouse chromosomes in somatic cell hybrids (thymidine kinase-lactate dehydrogenase A-isocitrate dehydrogenase-C-11,

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

Wilms' tumor in seven children with congenital aniridia.

Bilateral Wilms' tumour. Age at diagnosis, associated congenital anormalies, and possible pattern of inheritance.

Bilateral Wilms' tumor. A review.

Congenital anomalies in children with Wilms' tumor: a new survey.

Relation between cancer and congenital defects in man.

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

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685-690

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scholarly article

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10.1136/ADC.57.9.685

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9

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57

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1982-09-01T00:00:00Z

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6289758

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1627794

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