Literature DB >> 1415263

The need for care in the use of linkage analysis for genetic diagnosis in small families, with particular reference to uniparental disomy.

C G Woods, J H Edwards.   

Abstract

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Year:  1992        PMID： 1415263      PMCID： PMC1682845     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  3 in total

1.  Non-paternity and prenatal genetic screening.

Authors:  D J Brock; A E Shrimpton
Journal:  Lancet       Date:  1991-11-02       Impact factor: 79.321

2.  Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?

Authors:  R Voss; E Ben-Simon; A Avital; S Godfrey; J Zlotogora; J Dagan; Y Tikochinski; J Hillel
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

3.  Uniparental disomy as a mechanism for human genetic disease.

Authors:  J E Spence; R G Perciaccante; G M Greig; H F Willard; D H Ledbetter; J F Hejtmancik; M S Pollack; W E O'Brien; A L Beaudet
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025
  3 in total
  1 in total

1.  Low segregation ratios in autosomal recessive disorders.

Authors:  S Bundey; I D Young
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318
  1 in total

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