Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF-I receptor (IGF1R) gene.
about
A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia.Response to Growth Hormone Treatment in a Patient with Insulin-like Growth Factor 1 Receptor (IGF1R) Deletion.Three novel IGF1R mutations in microcephalic patients with prenatal and postnatal growth impairment.Heterozygous nonsense mutations near the C-terminal region of IGF1R in two patients with small-for-gestational-age-related short stature.IGF1R Gene Alterations in Small for Gestational Age (SGA) Children.
P2860
Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF-I receptor (IGF1R) gene.
description
2013 nî lūn-bûn
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年论文
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2013年论文
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name
Familial short stature and int ...... e IGF-I receptor (IGF1R) gene.
@en
type
label
Familial short stature and int ...... e IGF-I receptor (IGF1R) gene.
@en
prefLabel
Familial short stature and int ...... e IGF-I receptor (IGF1R) gene.
@en
P2093
P2860
P1476
Familial short stature and int ...... e IGF-I receptor (IGF1R) gene.
@en
P2093
Angel Ferrández-Longás
Antonio Carrascosa
Antonio de Arriba
Beatriz Puga
Esteban Mayayo
Eva Barrio
José I Labarta
Laura Audí
María T Calvo
Mónica Fernández-Cancio
P2860
P304
P356
10.1111/J.1365-2265.2012.04481.X
P577
2013-02-01T00:00:00Z