Literature DB >> 1427916

Regional localization of the highly polymorphic locus D11S533 on the linkage map of human chromosome 11q.

M Litt1, J H Eubanks, G A Evans, T Phromchotikul.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1427916     DOI: 10.1016/s0888-7543(05)80199-5

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


× No keyword cloud information.
  3 in total

1.  Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.

Authors:  S Iyengar; H Kalinsky; S Weiss; M Korostishevsky; M Sadeh; Y Zhao; K K Kidd; B Bonne-Tamir
Journal:  J Med Genet       Date:  1997-05       Impact factor: 6.318

2.  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

3.  Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.

Authors:  E M Petty; J S Green; S J Marx; R T Taggart; N Farid; A E Bale
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.