Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Item
http://www.wikidata.org/entity/Q33597984
Actinin-associated LIM protein: identification of a domain interaction between PDZ and spectrin-like repeat motifsMicroarray comparative genomic hybridization in prenatal diagnosis: a reviewDe novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpointsA radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.Exome Sequencing in Fetuses with Structural MalformationsMolecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.The 4q subtelomere harboring the FSHD locus is specifically anchored with peripheral heterochromatin unlike most human telomeresCurrent controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy.A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.
P2860

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Item
http://www.wikidata.org/entity/Q33597984
description
1990 nî lūn-bûn
@nan
1990 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Prenatal identification of a g ...... ation with muscular dystrophy.
@ast
Prenatal identification of a g ...... ation with muscular dystrophy.
@en
type
label
Prenatal identification of a g ...... ation with muscular dystrophy.
@ast
Prenatal identification of a g ...... ation with muscular dystrophy.
@en
prefLabel
Prenatal identification of a g ...... ation with muscular dystrophy.
@ast
Prenatal identification of a g ...... ation with muscular dystrophy.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P932
P356
P1433
P1476
Prenatal identification of a g ...... ation with muscular dystrophy.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P932