Literature DB >> 263447

Size and pericentric inversion heteromorphisms of secondary constriction regions (h) of chromosomes 1, 9, and 16 as detected by CBG technique in Caucasians: classification, frequencies, and incidence.

R S Verma, H Dosik, H A Lubs.   

Abstract

Eighty normal Caucasians were studied by CBG technique for estimation of size and inversion heteromorphisms of chromosomes 1, 9, and 16. Size heteromorphisms were classified into one of five sizes using 16p as a reference standard: very small, small, intermediate, large, and very large. Inversion heteromorphisms were also classified into 5 categories - eg, no inversion; partial inversion - minor; half inversion; partial inversion - major; and complete inversion. The frequencies of size heteromorphisms for chromosomes 1, 9, and 16 were 11.3%, 47.5%, and 7.5%, respectively. Thirty-four chromosomes were found to have inversions. Of these, 16 were in chromosome 1, and 18 were in chromosome 9. No inversions were found in chromosome 16. An increase in the size of the h region was more frequently associated with inversion, suggesting that there is a possible relationship between size and inversion. For example, there were 118 chromosomes that were classified as "intermediate" by size; 23 (19.5%) had inversions. In contrast, there were 225 that were "small" in size, and only 10 (4.4%) had inversions. There was no significant difference between males and females for size and position heteromorphisms.

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Year:  1978        PMID: 263447     DOI: 10.1002/ajmg.1320020403

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  9 in total

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Review 2.  Aspects of evaluation, significance, and evolution of human C-band heteromorphism.

Authors:  B Erdtmann
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3.  The quantitative analysis of constitutive heterochromatic regions of human chromosomes 1, 9, and 16 in relation to size and inversion heteromorphisms in East Indians.

Authors:  R S Verma; J Rodriguez; H Dosik
Journal:  Experientia       Date:  1982-03-15

4.  Quantitative analysis of C bands in chromosomes 1, 9, and 16 of Brazilian Indians and Caucasoids.

Authors:  B Erdtmann; F M Salzano; M S Mattevi; R Z Flores
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Molecular topography of the secondary constriction region (qh) of human chromosome 9 with an unusual euchromatic band.

Authors:  R S Verma; S Luke; J P Brennan; T Mathews; R A Conte; M J Macera
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

6.  Heterogeneity of human chromosome 9 constitutive heterochromatin as revealed by sequential distamycin A/DAPI staining and C-banding.

Authors:  C H Buys; W L Gouw; J A Blenkers; C H van Dalen
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Q- and C-band polymorphisms in patients with ovarian or breast carcinoma.

Authors:  S Kivi; A V Mikelsaar
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

8.  A homozygous NOP14 variant is likely to cause recurrent pregnancy loss.

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Journal:  J Hum Genet       Date:  2018-02-13       Impact factor: 3.172

9.  Parental chromosomal heteromorphisms are not associated with an increased risk of embryo aneuploidy.

Authors:  Carlos Hernandez-Nieto; Sonia Gayete-Lafuente; Tamar Alkon-Meadows; Joseph Lee; Martha Luna-Rojas; Tanmoy Mukherjee; Alan B Copperman; Benjamin Sandler
Journal:  JBRA Assist Reprod       Date:  2021-10-04
  9 in total

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