21 monosomy in a retarded female infant

21 monosomy in a retarded female infant

Item
http://www.wikidata.org/entity/Q33586312
Hypogammaglobulinaemia in a patient with ring chromosome 21Four new cases of ring 21 and 22 including familial transmission of ring 21.Human ETS2 gene on chromosome 21 is not rearranged in Alzheimer disease.Molecular genetics of human chromosome 21.Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 regionProximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development.Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literatureFunctional implications of differential chromosome banding.
P2860

21 monosomy in a retarded female infant

Item
http://www.wikidata.org/entity/Q33586312
description
1974 nî lūn-bûn
@nan
1974 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1974 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1974年の論文
@ja
1974年論文
@yue
1974年論文
@zh-hant
1974年論文
@zh-hk
1974年論文
@zh-mo
1974年論文
@zh-tw
1974年论文
@wuu
name
21 monosomy in a retarded female infant
@ast
21 monosomy in a retarded female infant
@en
21 monosomy in a retarded female infant.
@nl
type
label
21 monosomy in a retarded female infant
@ast
21 monosomy in a retarded female infant
@en
21 monosomy in a retarded female infant.
@nl
prefLabel
21 monosomy in a retarded female infant
@ast
21 monosomy in a retarded female infant
@en
21 monosomy in a retarded female infant.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P698
P932
P356
P1433
P1476
21 monosomy in a retarded female infant
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P698
P932