Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
about
Genetics and Genomics of Congenital Heart Disease.MEF2C loss-of-function mutation contributes to congenital heart defects.The genetics of congenital heart disease… understanding and improving long-term outcomes in congenital heart disease: a review for the general cardiologist and primary care physician.Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.
P2860
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 31 August 2016
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
@en
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
@nl
type
label
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
@en
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
@nl
prefLabel
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
@en
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.
@nl
P2093
P2860
P1476
Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans
@en
P2093
Alicia Braxton
Asha Rijhsinghani
Chelsea Kois
Christine M Eng
Donna M Muzny
Francesco Vetrini
James R Lupski
Jill A Rosenfeld
John W Belmont
Judy Holtzman
P2860
P304
P356
10.1016/J.AJHG.2016.07.011
P407
P577
2016-09-08T00:00:00Z