Literature DB >> 1923835

Dinucleotide repeat polymorphism at the D16S288 locus.

Y Shen1, K Holman, A Thompson, H Kozman, D F Callen, G R Sutherland, R I Richards.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1991        PMID： 1923835      PMCID： PMC328921          DOI： 10.1093/nar/19.19.5445

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


× No keyword cloud information.
  3 in total

1.  An expanded mouse-human hybrid cell panel for mapping human chromosome 16.

Authors:  D F Callen; E Baker; H J Eyre; S A Lane
Journal:  Ann Genet       Date:  1990

2.  Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

Authors:  R I Richards; Y Shen; K Holman; H Kozman; V J Hyland; J C Mulley; G R Sutherland
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

3.  Physical mapping of human chromosomes by repetitive sequence fingerprinting.

Authors:  R L Stallings; D C Torney; C E Hildebrand; J L Longmire; L L Deaven; J H Jett; N A Doggett; R K Moyzis
Journal:  Proc Natl Acad Sci U S A       Date:  1990-08       Impact factor: 11.205
  3 in total
  1 in total

1.  Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease).

Authors:  P E Taschner; N de Vos; A D Thompson; D F Callen; N Doggett; S E Mole; T P Dooley; P G Barth; M H Breuning
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.