Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot-Reference-Cited by-同舟云学术

Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot

Published:2003-09-24 Issue:5 Volume:22 Page:372-377
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Pizzuti Antonio,Sarkozy Anna,Newton Anthea L.,Conti Emanuela,Flex Elisabetta,Cristina Digilio Maria,Amati Francesca,Gianni Debora,Tandoi Caterina,Marino Bruno,Crossley Merlin,Dallapiccola Bruno

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

2. Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study

3. Distinct Domains of the GATA-1 Cofactor FOG-1 Differentially Influence Erythroid versus Megakaryocytic Maturation

4. Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresia

5. Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletion.

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