Literature DB >> 8589701

Germline mosaicism in a female who seemed to be a carrier by sequence analysis.

S S Sommer1, A Knöll, C R Greenberg, R P Ketterling.   

Abstract

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Year:  1995        PMID： 8589701     DOI： 10.1093/hmg/4.11.2181

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  4 in total

1.  Germline and somatic mosaicism in a female carrier of Hunter disease.

Authors:  R Froissart; I Maire; V Bonnet; T Levade; D Bozon
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

2.  Mutation rates in humans. I. Overall and sex-specific rates obtained from a population study of hemophilia B.

Authors:  P M Green; S Saad; C M Lewis; F Giannelli
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

3.  A de novo unequal cross-over mutation between CYP11B1 and CYP11B2 genes causes familial hyperaldosteronism type I.

Authors:  C A Carvajal; C B Stehr; P A González; E M Riquelme; T Montero; M J Santos; A M Kalergis; C E Fardella
Journal:  J Endocrinol Invest       Date:  2010-07-13       Impact factor: 4.256

Review 4.  Hemophilia B: molecular pathogenesis and mutation analysis.

Authors:  A C Goodeve
Journal:  J Thromb Haemost       Date:  2015-05-18       Impact factor: 5.824
  4 in total

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