Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.
about
CpG island in the region of an autosomal dominant polycystic kidney disease locus defines the 5' end of a gene encoding a putative proton channelSaturating the region of the polycystic kidney disease gene with NotI linking clones.Phenotype recognition. Clinicians' contributions to molecular genetics.Multipoint mapping of adult onset polycystic kidney disease (PKD1) on chromosome 16.Estimating locus heterogeneity in autosomal dominant polycystic kidney disease (ADPKD) in the Spanish populationMap of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.Haplotype analysis in autosomal dominant polycystic kidney diseaseReceptor protein tyrosine phosphatases are novel components of a polycystin complexMutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease.Evidence for linkage disequilibrium between D16S94 and the adult onset polycystic kidney disease (PKD1) gene.Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysisClinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complexClinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1).Construction of a map of chromosome 16 by using radiation hybridsCosmid walking and chromosome jumping in the region of PKD1 reveal a locus duplication and three CpG islandsDe novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I population.Diagnosis of adult polycystic kidney disease by genetic markers and ultrasonographic imaging in a voluntary family register.
P2860
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P2860
Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.
description
1990 nî lūn-bûn
@nan
1990 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի մայիսին 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
Identification of a locus whic ...... disease gene on chromosome 16.
@ast
Identification of a locus whic ...... disease gene on chromosome 16.
@en
type
label
Identification of a locus whic ...... disease gene on chromosome 16.
@ast
Identification of a locus whic ...... disease gene on chromosome 16.
@en
prefLabel
Identification of a locus whic ...... disease gene on chromosome 16.
@ast
Identification of a locus whic ...... disease gene on chromosome 16.
@en
P2093
P2860
P1476
Identification of a locus whic ...... disease gene on chromosome 16
@en
P2093
Germino GG
Nakamura Y
Reeders ST
P2860
P304
P407
P577
1990-05-01T00:00:00Z