Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance.
about
22q11 deletion syndrome: a genetic subtype of schizophrenia.Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two casesShould embryos with autosomal monosomy by preimplantation genetic testing for aneuploidy be transferred?: Implications for embryo selection from a systematic literature review of autosomal monosomy survivors.Compound phenotype in a girl with r(22), concomitant microdeletion 22q13.32-q13.33 and mosaic monosomy 22.unbalanced translocation t(15;22)(q26.2;q12) with velo-cardio-facial syndrome: A case report and review of the literature
P2860
Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance.
@en
type
label
Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance.
@en
prefLabel
Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance.
@en
P2093
P1476
Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance.
@en
P2093
Canto-Herrera J
Castillo-Zapata I
Ceballos-Quintal JM
Pinto-Escalante D
P2860
P304
P356
10.1002/(SICI)1096-8628(19980305)76:2<150::AID-AJMG8>3.0.CO;2-X
P577
1998-03-01T00:00:00Z