Literature DB >> 4232527

Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations.

F Hecht, M P Case, E W Lovrien, J V Higgins, H C Thuline, J Melnyk.   

Abstract

Lymphocytes from 20 individuals with Down's syndrome due to 13-15/21 centric-fusion translocations were studied by autoradiography after continuous late labeling with tritiated thymidine. In no case was chromosome 13 involved; chromosome 14 was involved in 18 cases, and chromosome 15 in two cases. These results are similar to those from 13 previously studied cases and indicate that the entry of chromosomes 13-15 into translocations is nonrandom. This nonrandomness is not a simple function of chromosome size or shape, since chromosomes 13-15 are acrocentrics of similar size.

Entities:  

Mesh:

Substances:

Year:  1968        PMID: 4232527     DOI: 10.1126/science.161.3839.371

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  22 in total

1.  Delineation of Robertsonian translocations in man by means of chromosome banding.

Authors:  F S Hill; R L Summitt
Journal:  Eur J Pediatr       Date:  1977-11-04       Impact factor: 3.183

2.  Translocation Down syndrome in Ohio 1970-1981: epidemiologic and cytogenetic factors and mutation rate estimates.

Authors:  L H Pulliam; C A Huether
Journal:  Am J Hum Genet       Date:  1986-09       Impact factor: 11.025

3.  Acrocentric associations in mongol populations.

Authors:  D J Curtis
Journal:  Humangenetik       Date:  1974-04-24

4.  Fluorescent staining of human chromosomes: identification of some common aberrations.

Authors:  I A Uchida; C C Lin
Journal:  Can Med Assoc J       Date:  1971-09-04       Impact factor: 8.262

Review 5.  Down's syndrome. Current stage of cytogenetic research.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971

6.  Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p).

Authors:  C G Palmer; P M Conneally; J C Christian
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

7.  Human karyotype polymorphism. I. Routine and fluorescence microscopic investigation of chromosomes in a normal adult population.

Authors:  A V Mikelsaar; S J Tüür; M E Käosaar
Journal:  Humangenetik       Date:  1973

8.  Quinacrine fluorescence patterns in somatic chromosomes of a t(15q15q) carrier.

Authors:  M C Yoshida; N Nomoto; M Sasaki
Journal:  Humangenetik       Date:  1972

9.  Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.

Authors:  F Hecht; W J Kimberling
Journal:  Am J Hum Genet       Date:  1971-07       Impact factor: 11.025

10.  Non-random association of human acrocentric chromosomes.

Authors:  S R Patil; H A Lubs
Journal:  Humangenetik       Date:  1971
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.