Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity
about
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalChanging clinical patterns and increasing prevalence in CADASIL.Mixture distributions in human genetics research.Molecular basis of genetic heterogeneity: role of the clinical neurologist.
P2860
Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity
description
1995 nî lūn-bûn
@nan
1995 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Hereditary multi-infarct demen ...... f probable locus heterogeneity
@ast
Hereditary multi-infarct demen ...... f probable locus heterogeneity
@en
type
label
Hereditary multi-infarct demen ...... f probable locus heterogeneity
@ast
Hereditary multi-infarct demen ...... f probable locus heterogeneity
@en
prefLabel
Hereditary multi-infarct demen ...... f probable locus heterogeneity
@ast
Hereditary multi-infarct demen ...... f probable locus heterogeneity
@en
P2093
P2860
P356
P1476
Hereditary multi-infarct demen ...... f probable locus heterogeneity
@en
P2093
P2860
P356
10.1136/JMG.32.1.57
P407
P577
1995-01-01T00:00:00Z