Literature DB >> 2216804

Dinucleotide repeat polymorphism at the D11S35 locus.

M Litt1, V Sharma, J A Luty.   

Abstract

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Year:  1990        PMID： 2216804      PMCID： PMC332371          DOI： 10.1093/nar/18.19.5921-a

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  2 in total

1.  A detailed genetic map of the long arm of chromosome 11.

Authors:  C Julier; Y Nakamura; M Lathrop; P O'Connell; M Leppert; M Litt; T Mohandas; J M Lalouel; R White
Journal:  Genomics       Date:  1990-07       Impact factor: 5.736

2.  Seven polymorphic loci mapping to human chromosomal region 11q22-qter.

Authors:  C L Maslen; C Jones; T Glaser; R E Magenis; R Sheehy; J Kellogg; M Litt
Journal:  Genomics       Date:  1988-01       Impact factor: 5.736
  2 in total
  10 in total

1.  Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.

Authors:  R A Spritz; K M Strunk; C L Hsieh; G S Sekhon; U Francke
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

2.  Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish population.

Authors:  J J Fuentes; I Banchs; V Volpini; X Estivill
Journal:  Int J Legal Med       Date:  1993       Impact factor: 2.686

3.  Genetic linkage analysis of 14 candidate gene loci in a family with autosomal dominant osteoarthritis without dysplasia.

Authors:  I Meulenbelt; C Bijkerk; F C Breedveld; P E Slagboom
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

4.  Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium.

Authors:  E Lange; A L Borresen; X Chen; L Chessa; S Chiplunkar; P Concannon; S Dandekar; S Gerken; K Lange; T Liang
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

5.  Absence of linkage to the ataxia telangiectasia locus in familial breast cancer.

Authors:  R Wooster; D Ford; J Mangion; B A Ponder; J Peto; D F Easton; M R Stratton
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

6.  Linkage analysis in Usher syndrome type I (USH1) families from Spain.

Authors:  C Espinós; C Nájera; J M Millán; C Ayuso; M Baiget; H Pérez-Garrigues; O Rodrigo; C Vilela; M Beneyto
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

7.  Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22-q24.

Authors:  G M Hampton; L A Penny; R N Baergen; A Larson; C Brewer; S Liao; R M Busby-Earle; A W Williams; C M Steel; C C Bird
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-19       Impact factor: 11.205

8.  Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q.

Authors:  E C Mariman; S E van Beersum; C W Cremers; F M van Baars; H H Ropers
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

9.  Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.

Authors:  J M Fletcher; K Evans; D Baillie; P Byrd; D Hanratty; S Leach; C Julier; J R Gosden; W Muir; D J Porteous
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

10.  Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations.

Authors:  J Gudmundsson; R B Barkardottir; G Eiriksdottir; T Baldursson; A Arason; V Egilsson; S Ingvarsson
Journal:  Br J Cancer       Date:  1995-09       Impact factor: 7.640
  10 in total

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