Literature DB >> 3136814

Haemophilia A: carrier detection by DNA analysis.

R Schwaab1, J Oldenburg, M Higuchi, M Ludwig, L Kochhan, J Horst, H H Brackmann, H Egli, K Olek.   

Abstract

From 46 families of predominantly German origin, afflicted with haemophilia A, 178 females were tested for carrier status. Two polymorphic restriction endonuclease sites, the extragenic marker locus DXS 52 (St 14 probe) and the intragenic Bcl I RFLP were investigated in these families. In some cases the results were corroborated by identifying (i) deletions within the factor VIII:C gene and (ii) eliminating a restriction endonuclease site. Two new alleles of the DXS 52 marker locus were found. According to this strategy, 27 women were classified as carriers and 74 as non-carriers. Forty-six women were classified as carriers according to pedigree analysis. Twenty-five females of families with sporadic cases and 6 test persons, who had mothers who where homozygous for the marker alleles, were diagnosed by additional use of conventional carrier detection.

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Year:  1988        PMID: 3136814     DOI: 10.1007/bf00319731

Source DB:  PubMed          Journal:  Blut        ISSN: 0006-5242


  19 in total

1.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

2.  Application of molecular genetics to prenatal diagnosis and carrier detection in the hemophilias: some limitations.

Authors:  J B Graham; P P Green; R A McGraw; L M Davis
Journal:  Blood       Date:  1985-10       Impact factor: 22.113

3.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

4.  Carrier detection in hemophilia A: a cooperative international study. II. The efficacy of a universal discriminant.

Authors:  P P Green; P M Mannucci; E Briët; R Ljung; C K Kasper; E M Essien; J Chediak; C R Rizza; J B Graham
Journal:  Blood       Date:  1986-06       Impact factor: 22.113

5.  Carrier detection in hemophilia A: a cooperative international study. I. The carrier phenotype.

Authors:  J B Graham; C R Rizza; J Chediak; P M Mannucci; E Briët; R Ljung; C K Kasper; E M Essien; P P Green
Journal:  Blood       Date:  1986-06       Impact factor: 22.113

6.  Concurrence of von Willebrand's disease and hemophilia A: implications for carrier detection and prevalence.

Authors:  C H Miller; M W Hilgartner; M B Harris; J B Bussel; L M Aledort
Journal:  Am J Med Genet       Date:  1986-05

7.  Molecular cloning of a cDNA encoding human antihaemophilic factor.

Authors:  J J Toole; J L Knopf; J M Wozney; L A Sultzman; J L Buecker; D D Pittman; R J Kaufman; E Brown; C Shoemaker; E C Orr
Journal:  Nature       Date:  1984 Nov 22-28       Impact factor: 49.962

8.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

9.  Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe.

Authors:  I Oberle; G Camerino; R Heilig; L Grunebaum; J P Cazenave; C Crapanzano; P M Mannucci; J L Mandel
Journal:  N Engl J Med       Date:  1985-03-14       Impact factor: 91.245

10.  Detection of carriers of classic hemophilia using an immunologic assay for antihemophilic factor (factor 8().

Authors:  T S Zimmerman; O D Ratnoff; A S Littell
Journal:  J Clin Invest       Date:  1971-01       Impact factor: 14.808

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  1 in total

1.  Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A.

Authors:  J Oldenburg; R Schwaab; T Grimm; K Zerres; P Hakenberg; H H Brackmann; K Olek
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

  1 in total

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