Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum development.
about
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic herniaAbsence makes the search grow longerThe same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplicationsGenomic characterization of chromosome 8 pericentric trisomy.Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture.Inverted duplication/deletion of chromosome 8p: mild clinical phenotype.Structural chromosomal abnormalities detected during CVS analysis and their role in the prenatal ascertainment of cryptic subtelomeric rearrangements
P2860
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P2860
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum development.
description
1994 nî lūn-bûn
@nan
1994 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի մարտին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Trisomy 8 syndrome owing to is ...... n corpus callosum development.
@ast
Trisomy 8 syndrome owing to is ...... n corpus callosum development.
@en
type
label
Trisomy 8 syndrome owing to is ...... n corpus callosum development.
@ast
Trisomy 8 syndrome owing to is ...... n corpus callosum development.
@en
prefLabel
Trisomy 8 syndrome owing to is ...... n corpus callosum development.
@ast
Trisomy 8 syndrome owing to is ...... n corpus callosum development.
@en
P2093
P2860
P356
P1476
Trisomy 8 syndrome owing to is ...... n corpus callosum development.
@en
P2093
A Giannotti
B Dallapiccola
C Danesino
F Uccellatore
G Floridia
M C Digilio
O Zuffardi
R Mingarelli
P2860
P304
P356
10.1136/JMG.31.3.238
P407
P577
1994-03-01T00:00:00Z