Literature DB >> 1511978

Fragile site (16) (q22). III. Segregation analysis.

B Müller1, W Feichtinger, C Bonaïti-Pellié, M Schmid.   

Abstract

The rare autosomal fragile site, fra (16) (q22), is the most common of all rare autosomal fragile sites and has a heterozygote frequency of about 5%. Evidence for it was found following the segregation expected from a simple codominant trait with complete penetrance; this is in contrast to a variety of other rare autosomal fragile sites. Based on the analysis of 12 families in which fra (16) (q22) is segregating, we found that, whereas complete penetrance could be confirmed, the transmitting parent was significantly more likely to be of the female sex. On the other hand, there was no evidence for preferential transmission to offspring of either sex.

Entities:  

Mesh:

Year:  1992        PMID: 1511978     DOI: 10.1007/bf00221948

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  4 in total

1.  The fragile site (16) (q22). I. Induction by AT-specific DNA-ligands and population frequency.

Authors:  M Schmid; W Feichtinger; A Jessberger; J Köhler; R Lange
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

2.  Demonstration of a heritable fragile site in human chromosome 16 with distamycin A.

Authors:  M Schmid; C Klett; A Niederhofer
Journal:  Cytogenet Cell Genet       Date:  1980

3.  Segregation analysis of rare autosomal fragile sites.

Authors:  S L Sherman; G R Sutherland
Journal:  Hum Genet       Date:  1986-02       Impact factor: 4.132

4.  Heritable fragile sites on human chromosomes. IX. Population cytogenetics and segregation analysis of the BrdU-requiring fragile site at 10q25.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.