about
Histogenesis of retinal dysplasia in trisomy 13Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeSemilobar Holoprosencephaly with Neurogenic Hypernatraemia: Two new cases.Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation.Genetically induced abnormal cranial development in human trisomy 18 with holoprosencephaly: comparisons with the normal tempo of osteogenic-neural development.Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մարտին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Molecular genetics of holoprosencephaly.
@ast
Molecular genetics of holoprosencephaly.
@en
type
label
Molecular genetics of holoprosencephaly.
@ast
Molecular genetics of holoprosencephaly.
@en
prefLabel
Molecular genetics of holoprosencephaly.
@ast
Molecular genetics of holoprosencephaly.
@en
P2093
P356
P1476
Molecular genetics of holoprosencephaly.
@en
P2093
P304
P356
10.2741/NANNI
P577
2000-03-01T00:00:00Z