Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.
about
CALL gene is haploinsufficient in a 3p- syndrome patientMisguided axonal projections, neural cell adhesion molecule 180 mRNA upregulation, and altered behavior in mice deficient for the close homolog of L1Del(3) (p25.3) without phenotypic effectClinical, cytogenetic and molecular study in a case of r(3) with 3p deletion and review of the literature.3p deletion syndrome: implications for cochlear implantation.A rare chromosome 3 imbalance and its clinical implications.Blepharophimosis-mental retardation syndrome and terminal deletion of chromosome 3p.Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery.
P2860
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P2860
Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Infant with del(3) (p25-pter): ...... of previously reported cases.
@ast
Infant with del(3) (p25-pter): ...... of previously reported cases.
@en
type
label
Infant with del(3) (p25-pter): ...... of previously reported cases.
@ast
Infant with del(3) (p25-pter): ...... of previously reported cases.
@en
prefLabel
Infant with del(3) (p25-pter): ...... of previously reported cases.
@ast
Infant with del(3) (p25-pter): ...... of previously reported cases.
@en
P2093
P356
P1476
Infant with del(3) (p25-pter): ...... of previously reported cases.
@en
P2093
P304
P356
10.1002/AJMG.1320440508
P577
1992-11-01T00:00:00Z