Literature DB >> 2861387

Factor VIII gene specific probe for prenatal diagnosis of haemophilia A.

N Din, M Schwartz, T Kruse, S R Vestergaard, P Ahrens, D Caput, K Hartog, M Quiroga.   

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Year:  1985        PMID： 2861387     DOI： 10.1016/s0140-6736(85)91873-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  A new HindIII restriction fragment length polymorphism in the hemophilia A locus.

Authors:  P Ahrens; T A Kruse; M Schwartz; P B Rasmussen; N Din
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

Review 2.  Diagnosis of genetic disease using recombinant DNA.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

3.  De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosis.

Authors:  M Delpech; N Deburgrave; M Baudis; P Maissonneuve; J M Bardin; Y Sultan; J C Kaplan
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132
  3 in total

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