GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.
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A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases.TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosusGenetic basis of aortic valvular disease.MEF2C loss-of-function mutation contributes to congenital heart defects.Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies.A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects.HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
P2860
Q33683998-99C66FD7-AA62-4AF6-B92A-8566BF1FFE04Q33702965-52B8A247-1880-4238-8E64-015BBBB5742AQ39117737-867E1FDA-666A-443E-82EA-F3EC15A725B2Q43466893-94C62B25-9A6B-49AA-95B4-A0D2E1BEC9D0Q47865347-C3271E8C-0C6C-4882-A13D-8CE3B2324480Q49814158-624022D9-55B1-4BB9-BA31-FA635BD7B68BQ51273200-C09CCD3D-0EF4-4AB1-B1CC-A5AA51877EB5
P2860
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.
description
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name
GATA5 mutation homozygosity li ...... enotype in a Lebanese patient.
@en
GATA5 mutation homozygosity li ...... enotype in a Lebanese patient.
@nl
type
label
GATA5 mutation homozygosity li ...... enotype in a Lebanese patient.
@en
GATA5 mutation homozygosity li ...... enotype in a Lebanese patient.
@nl
prefLabel
GATA5 mutation homozygosity li ...... enotype in a Lebanese patient.
@en
GATA5 mutation homozygosity li ...... enotype in a Lebanese patient.
@nl
P2093
P2860
P356
P1476
GATA5 mutation homozygosity li ...... henotype in a Lebanese patient
@en
P2093
Akl C Fahed
Fadi Bitar
Georges Nemer
Hadla Hariri
Inaam El-Rassy
Kameel Kassab
Lara Gharibeh
Manal Zein
P2860
P304
P356
10.1002/MGG3.190
P577
2015-12-20T00:00:00Z