(Q36792705)

16 August 2017

title

Single gene disorders associated with congenital diaphragmatic hernia (English)

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congenital diaphragmatic hernia

16 August 2017

0 references

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Anne M Slavotinek

1

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16 August 2017

publication date

1 May 2007

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American Journal of Medical Genetics Part C: Seminars in Medical Genetics

16 August 2017

published in

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16 August 2017

volume

145C

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16 August 2017

issue

2

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16 August 2017

page(s)

172-183

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Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome

16 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

A recurring FBN1 gene mutation in neonatal Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: patient report and review of the literature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

Congenital diaphragmatic hernia in WAGR syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.30125

21 January 2018

Identifiers

DOI

10.1002/AJMG.C.30125

1 reference

16 August 2017

1 reference