Implications of copy number variation in people with chromosomal abnormalities: potential for greater variation in copy number state may contribute to variability of phenotype.
about
Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach.The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome.A familial Cri-du-Chat/5p deletion syndrome resulted from rare maternal complex chromosomal rearrangements (CCRs) and/or possible chromosome 5p chromothripsis.
P2860
Implications of copy number variation in people with chromosomal abnormalities: potential for greater variation in copy number state may contribute to variability of phenotype.
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Implications of copy number va ...... e to variability of phenotype.
@ast
Implications of copy number va ...... e to variability of phenotype.
@en
Implications of copy number va ...... e to variability of phenotype.
@nl
type
label
Implications of copy number va ...... e to variability of phenotype.
@ast
Implications of copy number va ...... e to variability of phenotype.
@en
Implications of copy number va ...... e to variability of phenotype.
@nl
prefLabel
Implications of copy number va ...... e to variability of phenotype.
@ast
Implications of copy number va ...... e to variability of phenotype.
@en
Implications of copy number va ...... e to variability of phenotype.
@nl
P2093
P2860
P1433
P1476
Implications of copy number va ...... e to variability of phenotype.
@en
P2093
Adam J de Smith
Alexandra I F Blakemore
Anne L Trewick
P2860
P2888
P356
10.1007/S11568-010-9144-Z
P577
2010-08-10T00:00:00Z
P5875
P6179
1035803950