Literature DB >> 1916824

Linkage mapping and fluorescence in situ hybridization of TCTE1 on human chromosome 6p: analysis of dinucleotide polymorphisms on native gels.

T J Kwiatkowski1, A L Beaudet, B J Trask, H Y Zoghbi.   

Abstract

Highly informative dinucleotide repeat polymorphisms were identified at the T-complex-associated-testes-expressed-1 (TCTE1) locus on human chromosome 6p. Electrophoresis of single-stranded DNA on native gels facilitated the analysis of the dinucleotide polymorphisms. Linkage mapping positions this marker midway between the centromere and HLA with recombination fractions as follows: D6Z1-0.21-TCTE1-0.24-HLA. Two-color fluorescence in situ hybridization places TCTE1 proximal to CRIL171 (D6S19). Together, linkage and in situ hybridization indicate that the order of the loci is D6Z1-D6S4-D6S90-TCTE1-D6S19-D6S29-HL A-telomere. A sequence tagged site (STS) was established, and three yeast artificial chromosome (YAC) clones were identified for the TCTE1 locus.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1916824     DOI: 10.1016/0888-7543(91)90180-m

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  11 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Mouse chromosome 17.

Authors:  L M Silver; K Artzt; D Barlow; K Fischer-Lindahl; M F Lyon; J Klein; L Snyder
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 3.  Mouse chromosome 17.

Authors:  K Artzt; D Barlow; W F Dove; K Fischer-Lindahl; J Klein; M F Lyon; L M Silver
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

4.  Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity.

Authors:  R S Ramesar; J Greenberg; R Martin; R Goliath; S Bardien; S Mundlos; P Beighton
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

Review 5.  Major histocompatibility complex, t-complex, and leukemia.

Authors:  M T Dorak; A K Burnett
Journal:  Cancer Causes Control       Date:  1992-05       Impact factor: 2.506

6.  Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A.

Authors:  J T Hecht; Y Wang; B Connor; S H Blanton; S P Daiger
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

7.  Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.

Authors:  W P Whitehouse; M Rees; D Curtis; A Sundqvist; K Parker; E Chung; D Baralle; R M Gardiner
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

8.  Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.

Authors:  S A Jordan; G J Farrar; R Kumar-Singh; P Kenna; M M Humphries; V Allamand; E M Sharp; P Humphries
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

9.  Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex.

Authors:  N Tripodis; R Mason; S J Humphray; A F Davies; J A Herberg; J Trowsdale; D Nizetic; G Senger; J Ragoussis
Journal:  Genome Res       Date:  1998-06       Impact factor: 9.043

10.  Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.

Authors:  M J Abramowicz; M Andrien; E Dupont; H Dorchy; J Parma; L Duprez; F D Ledley; W Courtens; E Vamos
Journal:  J Clin Invest       Date:  1994-07       Impact factor: 14.808

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.