Literature DB >> 2570405

A BstXI polymorphism detected by the factor VIII genomic probe p.482.6 (F8C).

S A Taylor1, P J Bridge, D P Lillicrap.   

Abstract

Mesh：

Substances：

Year:  1989        PMID： 2570405      PMCID： PMC318325          DOI： 10.1093/nar/17.15.6426

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


× No keyword cloud information.
  3 in total

1.  A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A.

Authors:  K L Wion; E G Tuddenham; R M Lawn
Journal:  Nucleic Acids Res       Date:  1986-06-11       Impact factor: 16.971

2.  Characterization of the human factor VIII gene.

Authors:  J Gitschier; W I Wood; T M Goralka; K L Wion; E Y Chen; D H Eaton; G A Vehar; D J Capon; R M Lawn
Journal:  Nature       Date:  1984 Nov 22-28       Impact factor: 49.962

3.  The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

Authors:  M Purrello; B Alhadeff; D Esposito; P Szabo; M Rocchi; M Truett; F Masiarz; M Siniscalco
Journal:  EMBO J       Date:  1985-03       Impact factor: 11.598
  3 in total
  1 in total

1.  A new marker at DXS 115 useful for carrier detection in hemophilia A.

Authors:  M Wehnert; W Schröder; F H Herrmann
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.