Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect (Q80167710)

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29 December 2019

title

Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect (English)

1 reference

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29 December 2019

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2

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3

Chang Hyun Kang

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29 December 2019

author name string

Hee Yeon Cho

1

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29 December 2019

Woong-Han Kim

4

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29 December 2019

Il Soo Ha

5

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29 December 2019

Hae Il Cheong

6

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29 December 2019

Young Choi

7

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29 December 2019

publication date

25 August 2006

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29 December 2019

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29 December 2019

volume

21

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issue

12

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29 December 2019

page(s)

1909-1912

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https://scigraph.springernature.com/pub.10.1007/s00467-006-0273-5

29 December 2019

exact match

0 references

cites work

Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization

1 reference

12 December 2020

No evidence of WT1 gene mutations in children with congenital diaphragmatic hernia

1 reference

12 December 2020

Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins

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12 December 2020

Immunohistochemical diagnosis of epithelioid mesothelioma: an update

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12 December 2020

A clinical overview of WT1 gene mutations

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12 December 2020

Double vagina, cardiac, pulmonary, and other genital malformations with 46, XY karyotype

1 reference

12 December 2020

WT-1 is required for early kidney development

1 reference

12 December 2020

Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome

1 reference

12 December 2020

Congenital diaphragmatic hernia in WAGR syndrome.

1 reference

12 December 2020

The candidate Wilms' tumour gene is involved in genitourinary development

1 reference

12 December 2020

Report of another child with sex reversal and cardiac, pulmonary, and diaphragm defects

1 reference

12 December 2020

Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndrome

1 reference

12 December 2020

WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.

1 reference

12 December 2020

The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo.

1 reference

12 December 2020

WAGR syndrome: a clinical review of 54 cases

1 reference

12 December 2020

Infants with Bochdalek diaphragmatic hernia: sibling precurrence and monozygotic twin discordance in a hospital-based malformation surveillance program.

1 reference

12 December 2020

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

1 reference

12 December 2020

Diaphragmatic hernia in Denys-Drash syndrome

1 reference

12 December 2020

Phenotypically normal girl with male pseudohermaphroditism, hypoplastic left ventricle, lung aplasia, horseshoe kidney, and diaphragmatic hernia

1 reference

12 December 2020

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

1 reference

12 December 2020

The Wilms tumour gene WT1 is expressed in murine mesoderm-derived tissues and mutated in a human mesothelioma

1 reference

12 December 2020