Literature DB >> 4042396

Heritable fragility at 11q13 and 12q13.

D F Smeets, J M Scheres, T W Hustinx.   

Abstract

The chromosomes of two mentally retarded probands were investigated because they were suspected of having the fragile X syndrome. However two other fragilities were detected. In one patient a fra(11)(q13) was found and in the other a fra(12)(q13). Family studies revealed that both fragile sites were real heritable ones. Besides these two heritable fragile sites, the common fragile site at 3p14 was frequently observed. The effects of BUdR, FUdR and methotrexate on the frequency of the three fragilities were studied. The two heritable fragile sites differed from the common fragile site at 3p14 with respect to their inducibility by FUdR and methotrexate.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 4042396     DOI: 10.1111/j.1399-0004.1985.tb00374.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Studies on three rare fragile sites. 2q13, 12q13, and 17p12 segregating in one family.

Authors:  D R Romain; L M Columbano-Green; R H Smythe; R G Parfitt; O B Gebbie; C J Chapman
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

2.  CGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1.

Authors:  Birgitta Winnepenninckx; Kim Debacker; Jacqueline Ramsay; Dominique Smeets; Arie Smits; David R FitzPatrick; R Frank Kooy
Journal:  Am J Hum Genet       Date:  2006-12-12       Impact factor: 11.025

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.