Literature DB >> 903153

Classification of qh regions in human chromosomes 1, 9, and 16 by C-banding.

S R Patil, H A Lubs.   

Abstract

We present a classification for secondary constriction (qh) regions with C-banding technique in chromosomes 1, 9, and 16 by means of comparing them to the short arm of chromosome 16. It is simple and convenient and can be used routinely. It can be incorporated into the modified Paris nomenclature system.

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Year:  1977        PMID: 903153     DOI: 10.1007/bf00295805

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


  12 in total

1.  Human Q and C chromosomal variations: distribution and incidence.

Authors:  W H McKenzie; H A Lubs
Journal:  Cytogenet Cell Genet       Date:  1975

2.  The nature and inheritance of an elongated secondary constriction on chromosome 9 of man.

Authors:  P H Fitzgerald
Journal:  Cytogenet Cell Genet       Date:  1973

3.  Polymorphism of human C-band heterochromatin. I. Frequency of variants.

Authors:  A P Craig-Holmes; F B Moore; M W Shaw
Journal:  Am J Hum Genet       Date:  1973-03       Impact factor: 11.025

4.  An analysis of the technical variables in the production of C bands.

Authors:  W H McKenzie; H A Lubs
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

5.  Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication.

Authors:  J R Lobitz; B K McCaw; F Hecht
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

6.  Localization of heterochromatin in human chromosomes.

Authors:  F E Arrighi; T C Hsu
Journal:  Cytogenetics       Date:  1971

7.  Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.

Authors:  A P Craig-Holmes; F B Moore; M W Shaw
Journal:  Am J Hum Genet       Date:  1975-03       Impact factor: 11.025

8.  Letter: A1 and C9 marker chromosomes in children with combined minor and major malformations.

Authors:  J Kunze; G Mau
Journal:  Lancet       Date:  1975-02-01       Impact factor: 79.321

9.  1q plus variants in a normal adult population (one with a pericentric inversion).

Authors:  S Tüür; M Käosaar; A V Mikelsaar
Journal:  Humangenetik       Date:  1974

10.  C- and Q-band polymorphisms in the chromosomes of three human populations.

Authors:  K E Buckton; M L O'Riordan; P A Jacobs; J A Robinson; R Hill; H J Evans
Journal:  Ann Hum Genet       Date:  1976-07       Impact factor: 1.670

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  21 in total

1.  C-band polymorphisms of chromosome 9: quantification by Ce-bands.

Authors:  K Wahedi; I H Pawlowitzki
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

2.  Variability and familial transmission of constitutive heterochromatin of human chromosomes evaluated by the method of linear measurement.

Authors:  P Balícek; J Zizka; H Skalská
Journal:  Hum Genet       Date:  1978-06-27       Impact factor: 4.132

3.  A comment on the paper: reciprocal translocation and the Philadelphia chromosome by Jessie L. Watt and Brenda M. Page, Hum. Genet. 42, 163--170 (1978)

Authors:  R Berger; A Bernheim
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132

4.  Cancer family syndrome: cytogenetic investigations, in vitro tetraploidy, and biomarker studies in a large family.

Authors:  G Guanti; F Susca; G Cristofaro; M L Caruso; S Massari; R Porsia; A Stella; I Giorgio
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

5.  The quantitative analysis of polymorphism on human chromosomes 1,9,16, and Y. IV. Heterogeneity of a normal population.

Authors:  O A Podugolnikova; A P Korostelev
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

6.  Relationship of the variability of the heterochromatic regions of chromosomes 1, 9, 16, and Y to some anthropometric characteristics in children with embryopathies of unknown etiology and in children with Down syndrome.

Authors:  O A Podugolnikova; N M Grigorjeva; M G Blumina
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  A deletion of heterochromatin only of the Y chromosome in an azoospermic male.

Authors:  G Cohen; A Manuel; M Cohen; K Fagan; H Grunstein
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  An attempt to define 1qh+, 9qh+, and 16qh+.

Authors:  U Friedrich; A J Therkelsen
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

9.  Polymorphism of human chromosomes 1, 9, 16, Y: variations, segregation and mosaicism.

Authors:  S Simi; F Tursi
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

10.  Constitutive heterochromatin studies in patients with solid tumors.

Authors:  S Suciu
Journal:  J Cancer Res Clin Oncol       Date:  1986       Impact factor: 4.553

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