Literature DB >> 12195713

11 hemophilia A patients without mutations in the factor VIII encoding gene.

N Klopp, J Oldenburg, C Uen, R Schneppenheim, J Graw.   

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Year:  2002        PMID： 12195713

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN： 0340-6245            Impact factor:   5.249


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  5 in total

1.  Utility of multiplex ligation-dependent probe amplification (MLPA) for hemophilia mutation screening.

Authors:  A B Payne; C J Bean; W C Hooper; C H Miller
Journal:  J Thromb Haemost       Date:  2012-09       Impact factor: 5.824

2.  Clinical utility gene card for: haemophilia A.

Authors:  Steve Keeney; Tony Cumming; P Vincent Jenkins; James S O'Donnell; Michael J Nash
Journal:  Eur J Hum Genet       Date:  2011-06-08       Impact factor: 4.246

3.  Evaluation of factor VIII polymorphic short tandem repeat markers in linkage analysis for carrier diagnosis of hemophilia A.

Authors:  Sabina Shrestha; Sufang Dong; Zuhua Li; Zhuliang Huang; Fang Zheng
Journal:  Biomed Rep       Date:  2016-07-04

4.  In silico profiling of deleterious amino acid substitutions of potential pathological importance in haemophlia A and haemophlia B.

Authors:  George Priya Doss C
Journal:  J Biomed Sci       Date:  2012-03-16       Impact factor: 8.410

5.  Identification of deep intronic individual variants in patients with hemophilia A by next-generation sequencing of the whole factor VIII gene.

Authors:  Hiroshi Inaba; Keiko Shinozawa; Kagehiro Amano; Katsuyuki Fukutake
Journal:  Res Pract Thromb Haemost       Date:  2017-08-05
  5 in total

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