Literature DB >> 7153496

Simple segregation analysis: a review of its history and terminology.

F W Nicholas.   

Abstract

The history of simple segregation analysis is reviewed with the aim of clarifying the present confusion in terminology. Although Weinberg's contribution to simple segregation analysis is considerable, it is noted that he was not responsible for one of the methods often attributed to him. For the benefit of biologists attempting to understand simple segregation analysis, the various names given by different authors to some of the methods of segregation analysis that are still in use are incorporated into a table. All the confusion in terminology can be avoided, however, by using an extension (due to Davie) of the singles method that combines a very simple and efficient estimate of segregation frequency with a very quick and simple estimate of its variance, and that is valid for all levels of ascertainment.

Mesh:

Year:  1982        PMID: 7153496     DOI: 10.1093/oxfordjournals.jhered.a109695

Source DB:  PubMed          Journal:  J Hered        ISSN: 0022-1503            Impact factor:   2.645


  6 in total

1.  Segregation analysis in Shwachman-Diamond syndrome: evidence for recessive inheritance.

Authors:  H Ginzberg; J Shin; L Ellis; S Goobie; J Morrison; M Corey; P R Durie; J M Rommens
Journal:  Am J Hum Genet       Date:  2000-03-14       Impact factor: 11.025

2.  C. C. Li (1912-2003): his science and his spirit.

Authors:  Partha P Majumder
Journal:  J Genet       Date:  2004-04       Impact factor: 1.166

3.  Autosomal dominant inheritance of centrotemporal sharp waves in rolandic epilepsy families.

Authors:  Bhavna Bali; Lewis L Kull; Lisa J Strug; Tara Clarke; Peregrine L Murphy; Cigdem I Akman; David A Greenberg; Deb K Pal
Journal:  Epilepsia       Date:  2007-07-28       Impact factor: 5.864

4.  Duchenne muscular dystrophy. Frequency of sporadic cases.

Authors:  G A Danieli; G Barbujani
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  Familial Aggregation of Aortic Valvular Stenosis: A Nationwide Study of Sibling Risk.

Authors:  Andreas Martinsson; Xinjun Li; Bengt Zöller; Pontus Andell; Charlotte Andersson; Kristina Sundquist; J Gustav Smith
Journal:  Circ Cardiovasc Genet       Date:  2017-12

6.  National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology.

Authors:  D Morrison; D FitzPatrick; I Hanson; K Williamson; V van Heyningen; B Fleck; I Jones; J Chalmers; H Campbell
Journal:  J Med Genet       Date:  2002-01       Impact factor: 6.318

  6 in total

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