Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report.

about

De Novo Duplication of 11p15 Associated With Congenital Diaphragmatic Hernia.

P2860

Q55383719-8F9689F2-4E1C-494E-90AE-55A349208969

P2860

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report.

Item

http://www.wikidata.org/entity/Q36758515

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Familial tetrasomy 4q35.2 asso ...... renal agenesis: a case report.

@ast

Familial tetrasomy 4q35.2 asso ...... renal agenesis: a case report.

@en

type

Item

label

Familial tetrasomy 4q35.2 asso ...... renal agenesis: a case report.

@ast

Familial tetrasomy 4q35.2 asso ...... renal agenesis: a case report.

@en

prefLabel

Familial tetrasomy 4q35.2 asso ...... renal agenesis: a case report.

@ast

Familial tetrasomy 4q35.2 asso ...... renal agenesis: a case report.

@en

P1476

Familial tetrasomy 4q35.2 asso ...... renal agenesis: a case report.

@en

P2093

Andreas Müller

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

Florian Kipfmüller

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

Heiko Reutter

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

Nicolai Kohlschmidt

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

Thomas Bogs

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

Ulrich Gembruch

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

P2860

Fog2 is required for normal diaphragm and lung development in mice and humans

A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation

Congenital diaphragmatic hernia with probable autosomal recessive inheritance in an extended consanguineous Pakistani pedigree.

Genetic aspects of human congenital diaphragmatic hernia.

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

Clinical variability of the 22q11.2 duplication syndrome.

De novo interstitial duplication 4(q28.1q35) associated with choanal atresia.

De novo copy number variants are associated with congenital diaphragmatic hernia.

The long-term follow-up of patients with a congenital diaphragmatic hernia: a broad spectrum of morbidity.

P2888

s13256-016-0855-1

P304

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

P31

scholarly article

P356

10.1186/S13256-016-0855-1

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

P407

English

P478

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

P577

2016-03-30T00:00:00Z

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

P6179

1049605932

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

P698

27036947

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

P921

congenital diaphragmatic hernia

birth defect

P932

4818464

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

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report.

about

P2860

P2860

Familial tetrasomy 4q35.2 associated with congenital diaphragmatic hernia and unilateral renal agenesis: a case report.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P478

P577

P6179

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P478

P577

P6179

P698

P921

P932