Prevalence And Penetrance Of Zfpm2 Mutations And Deletions Causing Congenital Diaphragmatic Hernia

Title

Prevalence And Penetrance Of Zfpm2 Mutations And Deletions Causing Congenital Diaphragmatic Hernia

Creator

Longoni M; Russell M K; High F A; Darvishi K; Maalouf F I; Kashani A; Tracy A A; Coletti C M; Loscertales M; Lage K; Ackerman K G; Woods S A; Ward-Melver C; Andrews D; Lee C; Pober B R; Donahoe P K

Publisher

Clinical Genetics

Date

2015
2015-04

Subject

congenital diaphragmatic hernia; defects; DNA copy number variation; exome; fallot; FOG2; FOG2; gene; Genetics & Heredity; penetrance; tetralogy; variants; ZFPM2

Identifier

Format

Journal Article or Conference Abstract Publication

Search for Full-text

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Rights

Article information provided for research and reference use only. All rights are retained by the journal listed under publisher and/or the creator(s).

Pages

362-367

Issue

4

Volume

87

Citation

Longoni M; Russell M K; High F A; Darvishi K; Maalouf F I; Kashani A; Tracy A A; Coletti C M; Loscertales M; Lage K; Ackerman K G; Woods S A; Ward-Melver C; Andrews D; Lee C; Pober B R; Donahoe P K, “Prevalence And Penetrance Of Zfpm2 Mutations And Deletions Causing Congenital Diaphragmatic Hernia,” NEOMED Bibliography Database, accessed June 13, 2021, https://neomed.omeka.net/items/show/9822.

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