Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia.
about
Combined pituitary hormone deficiency: current and future status.Genetic regulation of pituitary gland development in human and mouseCranial diabetes insipidus with pituitary stalk lesions.Identification of HESX1 mutations in Kallmann syndrome.Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
P2860
Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Heterozygous mutation of HESX1 ...... ures of septo-optic dysplasia.
@en
Heterozygous mutation of HESX1 ...... ures of septo-optic dysplasia.
@nl
type
label
Heterozygous mutation of HESX1 ...... ures of septo-optic dysplasia.
@en
Heterozygous mutation of HESX1 ...... ures of septo-optic dysplasia.
@nl
prefLabel
Heterozygous mutation of HESX1 ...... ures of septo-optic dysplasia.
@en
Heterozygous mutation of HESX1 ...... ures of septo-optic dysplasia.
@nl
P2093
P2860
P356
P1476
Heterozygous mutation of HESX1 ...... ures of septo-optic dysplasia.
@en
P2093
S Bernasconi
P2860
P2888
P304
P356
10.1007/BF03346416
P577
2008-08-01T00:00:00Z