Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter.
about
An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometryA unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies.Transforming Theory into Preventive Genetics in rural Communities.A syndrome of retinitis pigmentosa, congenital ichthyosis, hypergonadotropic hypogonadism, small stature, mental retardation, cranial dysmorphism, and abnormal electroencephalogram.
P2860
Familial X-linked ichthyosis, steroid sulfatase deficiency, mental retardation, and nullisomy for Xp223-pter.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh-hant
name
Familial X-linked ichthyosis, ...... and nullisomy for Xp223-pter.
@en
Familial X-linked ichthyosis, ...... and nullisomy for Xp223-pter.
@nl
type
label
Familial X-linked ichthyosis, ...... and nullisomy for Xp223-pter.
@en
Familial X-linked ichthyosis, ...... and nullisomy for Xp223-pter.
@nl
prefLabel
Familial X-linked ichthyosis, ...... and nullisomy for Xp223-pter.
@en
Familial X-linked ichthyosis, ...... and nullisomy for Xp223-pter.
@nl
P2093
P1433
P1476
Familial X-linked ichthyosis, ...... and nullisomy for Xp223-pter.
@en
P2093
P304
P356
10.1001/ARCHDERM.1985.01660120050018
P577
1985-12-01T00:00:00Z