Literature DB >> 1971099

Dinucleotide repeat polymorphism at the D1S104 locus.

J L Weber1, A E Kwitek, P E May.   

Abstract

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Year:  1990        PMID： 1971099      PMCID： PMC330796     

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


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  1 in total

1.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025
  1 in total
  5 in total

1.  Absence of linkage between idiopathic dilated cardiomyopathy and candidate genes involved in the immune function in a large Italian pedigree.

Authors:  M Krajinovic; L Mestroni; G M Severini; B Pinamonti; F Camerini; A Falaschi; M Giacca
Journal:  J Med Genet       Date:  1994-10       Impact factor: 6.318

2.  Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

Authors:  S B Cassidy; L W Lai; R P Erickson; L Magnuson; E Thomas; R Gendron; J Herrmann
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

3.  Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1.

Authors:  E C Mariman; A A Gabreëls-Festen; S E van Beersum; P J Jongen; H H Ropers; F J Gabreëls
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

4.  Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies.

Authors:  E C Mariman; A A Gabreëls-Festen; S E van Beersum; P J Jongen; E van de Looij; F Baas; P A Bolhuis; H H Ropers; F J Gabreëls
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

5.  Subchromosomal mapping of a putative transformation suppressor gene on human chromosome 1.

Authors:  I Horikawa; H Yamada; H Kugoh; Y Yuasa; M Suzuki; M Oshimura
Journal:  Jpn J Cancer Res       Date:  1995-05
  5 in total

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