De novo frameshift mutation in COUP-TFII (NR2F2) in human congenital diaphragmatic hernia.
about
Abnormal Paraventricular Nucleus of Hypothalamus and Growth Retardation Associated with Loss of Nuclear Receptor Gene COUP-TFIIGenetic disorders of nuclear receptors.Congenital diaphragmatic hernias: from genes to mechanisms to therapies.Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children.Systematic analysis of copy number variation associated with congenital diaphragmatic hernia.
P2860
De novo frameshift mutation in COUP-TFII (NR2F2) in human congenital diaphragmatic hernia.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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name
De novo frameshift mutation in ...... ngenital diaphragmatic hernia.
@en
De novo frameshift mutation in COUP-TFII
@nl
type
label
De novo frameshift mutation in ...... ngenital diaphragmatic hernia.
@en
De novo frameshift mutation in COUP-TFII
@nl
prefLabel
De novo frameshift mutation in ...... ngenital diaphragmatic hernia.
@en
De novo frameshift mutation in COUP-TFII
@nl
P2093
P2860
P356
P1476
De novo frameshift mutation in ...... ngenital diaphragmatic hernia.
@en
P2093
Carol J Bult
Frances A High
Jay M Wilson
Mauro Longoni
Patricia K Donahoe
Pooja Bhayani
P2860
P304
P356
10.1002/AJMG.A.37830
P407
P577
2016-07-01T00:00:00Z