Literature DB >> 3661566

Merging autosomal dominance and recessivity.

G B Van Ommen.   

Abstract

Mesh：

Substances：

Year:  1987        PMID： 3661566      PMCID： PMC1684309     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  2 in total

1.  The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24.

Authors:  F Baas; H Bikker; A Geurts van Kessel; R Melsert; P L Pearson; J J de Vijlder; G J van Ommen
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele.

Authors:  F Baas; H Bikker; G J van Ommen; J J de Vijlder
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
  2 in total
  2 in total

Review 1.  Human chromosome 8.

Authors:  S Wood
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

2.  Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.

Authors:  K E De Rooij; P A De Koning Gans; M I Skraastad; R D Belfroid; M Vegter-Van Der Vlis; R A Roos; E Bakker; G J Van Ommen; J T Den Dunnen; M Losekoot
Journal:  J Med Genet       Date:  1993-12       Impact factor: 6.318
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.