Genetic aspects of autosomal dominant late onset cerebellar ataxia.
about
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10Genomic imprinting: review and relevance to human diseases.Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting.Genetic study of indirect inguinal hernia.Can molecular imprinting explain heterozygote deficiency and hybrid vigor?Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I.Familial cerebellar ataxia and possible cosegregation with an inversion in chromosome 4
P2860
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P2860
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
description
1981 nî lūn-bûn
@nan
1981 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1981 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1981年の論文
@ja
1981年学术文章
@wuu
1981年学术文章
@zh-cn
1981年学术文章
@zh-hans
1981年学术文章
@zh-my
1981年学术文章
@zh-sg
1981年學術文章
@yue
name
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
@ast
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
@en
type
label
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
@ast
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
@en
prefLabel
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
@ast
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
@en
P2860
P1476
Genetic aspects of autosomal dominant late onset cerebellar ataxia.
@en
P2093
Harding AE
P2860
P304
P407
P577
1981-12-01T00:00:00Z