French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion
about
Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure.Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeatFounder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.Normal variation at the myotonic dystrophy locus in global human populations.Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutation.Carrell-Krusen Symposium Invited Lecture-1997. Myotonic disorders in childhood: diagnosis and treatment.
P2860
French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion
description
1994 nî lūn-bûn
@nan
1994 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
French myotonic dystrophy fami ...... h an intragenic 1 kb insertion
@ast
French myotonic dystrophy fami ...... h an intragenic 1 kb insertion
@en
type
label
French myotonic dystrophy fami ...... h an intragenic 1 kb insertion
@ast
French myotonic dystrophy fami ...... h an intragenic 1 kb insertion
@en
prefLabel
French myotonic dystrophy fami ...... h an intragenic 1 kb insertion
@ast
French myotonic dystrophy fami ...... h an intragenic 1 kb insertion
@en
P2093
P2860
P50
P356
P1476
French myotonic dystrophy fami ...... h an intragenic 1 kb insertion
@en
P2093
C Bonaïti-Pellié
H Hofmann-Radvanyi
I Dehaupas
P Shelbourne
P2860
P356
10.1136/JMG.31.1.33
P407
P577
1994-01-01T00:00:00Z