A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.
about
Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus
P2860
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.
@en
type
label
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.
@en
prefLabel
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.
@en
P2093
P2860
P1476
A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.
@en
P2093
Wainwright B
Williamson R
P2860
P304
P407
P577
1986-10-01T00:00:00Z