Literature DB >> 2569705

Accurate prenatal diagnosis with novel polymerase chain reaction primers in a family with sporadic hemophilia A.

G Sarkar1, M I Evans, S Kogan, J Lusher, S S Sommer.   

Abstract

Novel oligonucleotide primers are described for the convenient and internally controlled detection of the BclI factor VIII polymorphism on agarose gels. The primers were used for prenatal diagnosis in a family in which only one individual was affected with hemophilia A. In such families, it is important for the mother to understand that uncertainty about the point of origin of the mutation precludes the accurate diagnosis of affected fetuses but does allow the accurate diagnosis of unaffected fetuses in many cases.

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Year:  1989        PMID: 2569705

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  1 in total

1.  Identification of mutations in two families with sporadic hemophilia A.

Authors:  C Paynton; G Sarkar; S S Sommer
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

  1 in total

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