Literature DB >> 5087725

Use of genetic linkage for the detection of female carriers of hemophilia.

P R McCurdy.   

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Year:  1971        PMID： 5087725     DOI： 10.1056/NEJM197107222850409

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  5 in total

1.  A strategy for using multiple linked markers for genetic counseling.

Authors:  A Chakravarti; K H Buetow
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

2.  X-chromosome inactivation in human liver: confirmation of X-linkage of ornithine transcarbamylase.

Authors:  F C Ricciuti; T D Gelehrter; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1976-07       Impact factor: 11.025

3.  Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium.

Authors:  A Chakravarti
Journal:  Am J Hum Genet       Date:  1983-07       Impact factor: 11.025

4.  Prenatal diagnosis by linkage: hemophilia A and polymorphic glucose-6-phosphate deydrogenase.

Authors:  C J Edgell; H N Kirkman; E Clemons; P D Buchanan; C H Miller
Journal:  Am J Hum Genet       Date:  1978-01       Impact factor: 11.025

5.  Sequence variation data of F8 and F9 genes in functionally validated control individuals: implications on the molecular diagnosis of hemophilia.

Authors:  Ja Young Seo; Mi-Ae Jang; Hee-Jung Kim; Ki-O Lee; Sun-Hee Kim; Hee-Jin Kim
Journal:  Blood Res       Date:  2013-09-25
  5 in total

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