Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome
about
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnanciesDiffering Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis.Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
P2860
Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome
@en
type
label
Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome
@en
prefLabel
Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome
@en
P2093
P2860
P356
P1476
Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome
@en
P2093
Anne C Tabet
Anne L Delezoïde
Arnaud Molin
Celine Dupont
Demetrio Baldo
Enzo Troilo
Eva Pompilii
Federico Maggi
Francesca R Grati
Gabriella Bracalente
P2860
P356
10.1002/CCR3.48
P50
P577
2014-02-06T00:00:00Z