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Literature DB >> 3435045

Chi-squared tests with small numbers.

C A Smith¹.

Abstract

Mesh：

Year: 1986 PMID： 3435045 DOI： 10.1111/j.1469-1809.1986.tb01035.x

Source DB: PubMed Journal: Ann Hum Genet ISSN： 0003-4800 Impact factor: 1.670

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9 in total

1. Hardy-Weinberg testing of a single homozygous genotype.

Authors: John J Chen; Tao Duan; Richard Single; Kristie Mather; Glenys Thomson
Journal: Genetics Date: 2005-05-23 Impact factor: 4.562

2. Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.

Authors: John V Raelson; Randall D Little; Andreas Ruether; Hélène Fournier; Bruno Paquin; Paul Van Eerdewegh; W E C Bradley; Pascal Croteau; Quynh Nguyen-Huu; Jonathan Segal; Sophie Debrus; René Allard; Philip Rosenstiel; Andre Franke; Gunnar Jacobs; Susanna Nikolaus; Jean-Michel Vidal; Peter Szego; Nathalie Laplante; Hilary F Clark; René J Paulussen; John W Hooper; Tim P Keith; Abdelmajid Belouchi; Stefan Schreiber
Journal: Proc Natl Acad Sci U S A Date: 2007-09-05 Impact factor: 11.205

3. A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

Authors: J Zielenski; D Markiewicz; F Rininsland; J Rommens; L C Tsui
Journal: Am J Hum Genet Date: 1991-12 Impact factor: 11.025

9. Fragile sites and chromosome instability: the distribution of breaks induced by cis-diamine-dichloro-platinum (II) in Fanconi anemia lymphocyte cultures.

Authors: B Porfirio; D Smeets; L Beckers; D Caporossi; B Tedeschi; P Vernole; H Joenje; B Nicoletti; B Dallapiccola
Journal: Hum Genet Date: 1991-01 Impact factor: 4.132

9 in total

Chi-squared tests with small numbers.

1. Hardy-Weinberg testing of a single homozygous genotype.

2. Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.

3. A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

4. Forensic evaluation of HUMCD4: an Italian database.

5. Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.

6. Identifying chromosomal fragile sites from individuals: a multinomial statistical model.

7. Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.

8. Mating system and multilocus associations in a natural population of Pseudotsuga menziesii (Mirb.) Franco.

9. Fragile sites and chromosome instability: the distribution of breaks induced by cis-diamine-dichloro-platinum (II) in Fanconi anemia lymphocyte cultures.