Literature DB >> 2873459

Diagnosis of haemophilia B carriers using intragenic oligonucleotide probes.

P R Winship, G G Brownlee.   

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Year:  1986        PMID： 2873459     DOI： 10.1016/s0140-6736(86)92513-4

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


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  11 in total

1.  Prenatal diagnosis of haemophilia B by the use of polymerase chain reaction and direct sequencing.

Authors:  M Ludwig; H H Brackmann; K Olek
Journal:  Klin Wochenschr       Date:  1991-03-18

2.  MspI polymorphic site within the factor IX gene. Localization of the site and an improved method for detection.

Authors:  D L Freedenberg; S H Chen; K Kurachi; C R Scott
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

3.  Diagnosis of haemophilia B using the polymerase chain reaction.

Authors:  J Reiss; U Neufeldt; K Wieland; B Zoll
Journal:  Blut       Date:  1990-01

4.  Functionally important regions of the factor IX gene have a low rate of polymorphism and a high rate of mutation in the dinucleotide CpG.

Authors:  D D Koeberl; C D Bottema; J M Buerstedde; S S Sommer
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

5.  A DNA marker closely linked to the factor IX (haemophilia B) gene.

Authors:  L Mulligan; J J Holden; B N White
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

6.  Factor IX gene mutations causing haemophilia B: comparison of SSC screening versus systematic DNA sequencing and diagnostic applications.

Authors:  P Aguilar-Martinez; M C Romey; J F Schved; J C Gris; J Demaille; M Claustres
Journal:  Hum Genet       Date:  1994-09       Impact factor: 4.132

Review 7.  Haemophilia: strategies for carrier detection and prenatal diagnosis.

Authors:  I R Peake; D P Lillicrap; V Boulyjenkov; E Briet; V Chan; E K Ginter; E M Kraus; R Ljung; P M Mannucci; K Nicolaides
Journal:  Bull World Health Organ       Date:  1993       Impact factor: 9.408

8.  Recurrent mutations in the factor IX gene: founder effect or repeat de novo events. Investigation of the German haemophilia B population and review of de novo mutations.

Authors:  O Knobloch; B Zoll; K Zerres; H H Brackmann; K Olek; M Ludwig
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

9.  Parental origin of factor IX gene mutations, and their distribution in the gene.

Authors:  M Ludwig; T Grimm; H H Brackmann; K Olek
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

Review 10.  The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B.

Authors:  A H Bröcker-Vriends; E Bakker; H H Kanhai; G J van Ommen; P H Reitsma; J J van de Kamp; E Briët
Journal:  Ann Hematol       Date:  1992-01       Impact factor: 3.673
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