Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors-Reference-Cited by-同舟云学术

Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors

Published:1992-09 Issue:1 Volume:14 Page:144-152
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Tomfohrde James,Wood Stephen,Schertzer Michael,Wagner Michael J.,Wells Dan E.,Parrish Julia,Sadler Lori A.,Blanton Susan H.,Daiger Stephen P.,Wang Zhenyuan,Wilkie Patricia J.,Weber James L.

Publisher

Elsevier BV

Subject

Genetics

Reference34 articles.

1. Deletion mapping of chromosomes 8, 10, and 16 in human prostatic carcinoma;Bergerheim;Genes Chrom. Cancer,1991

2. Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8;Blanton;Genomics,1991

3. Influence of aberrant observations on high-resolution linkage analysis outcomes;Buetow;Am. J. Hum. Genet.,1991

4. A new StyI RFLP and haplotypes with the HindIII RFLP at the D8S5 (TL11) locus;Cottingham;Nucleic Acids Res,1991

5. An anonymous human single copy genomic clone (D8S5) (TL11) on chromosome 8 identifies a moderately frequent RFLP;Dietzsch;Nucleic Acids Res,1986

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