» Articles » PMID: 7218278

New C Band Markers of Human Chromosomes: C Band Position Variants

Overview
Journal J Med Genet
Specialty Genetics
Date 1980 Oct 1
PMID 7218278
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Although it is well known that variations in size are common in the centric heterochromatin of human chromosomes, it has not been appreciated that centric heterochromatin may be positioned either entirely on the short arm, centrally, or entirely on the long arm. Inspection of C banded karyotypes in which chromosomes were identified by previous Q banding showed C band position variants in all of the chromosomes of groups A, B, C, E, and F. These 'new' C band markers were followed in families and found to be heritable. By scoring chromosomes for both size and position of C bands it should be possible to distinguish the majority of homologous chromosomes in most people. The ease of scoring and high frequency of variation should make C band position variants extremely useful in linkage studies and population surveys.

Citing Articles

Partial inversion of the secondary constriction of chromosome 9. Does it exist?.

Mattei M, Mattei J, Guichaoua M, Giraud F Hum Genet. 1981; 59(4):310-6.

PMID: 7333585 DOI: 10.1007/BF00295463.


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

Erdtmann B Hum Genet. 1982; 61(4):281-94.

PMID: 6759365 DOI: 10.1007/BF00276592.


Gene mapping studies with the syndrome of autism.

Spence M, Ritvo E, Marazita M, Funderburk S, Sparkes R, Freeman B Behav Genet. 1985; 15(1):1-13.

PMID: 3985910 DOI: 10.1007/BF01071928.


AluI-resistant chromatin of chromosome 18: classification, frequencies and implications.

Babu A, Verma R, Patil S Chromosoma. 1987; 95(3):163-6.

PMID: 3038486 DOI: 10.1007/BF00330345.


A new approach in recognition of heterochromatic regions of human chromosomes by means of restriction endonucleases.

Babu A, Agarwal A, Verma R Am J Hum Genet. 1988; 42(1):60-5.

PMID: 2827464 PMC: 1715309.


References
1.
Arrighi F, Hsu T . Localization of heterochromatin in human chromosomes. Cytogenetics. 1971; 10(2):81-6. DOI: 10.1159/000130130. View

2.
Moore F, Shaw M . Polymorphism of human C-band heterochromatin. I. Frequency of variants. Am J Hum Genet. 1973; 25(2):181-92. PMC: 1762502. View

3.
del Solar C, UCHIDA I . Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis. J Pediatr. 1974; 84(4):534-8. DOI: 10.1016/s0022-3476(74)80673-6. View

4.
McKenzie W, Lubs H . Human Q and C chromosomal variations: distribution and incidence. Cytogenet Cell Genet. 1975; 14(2):97-115. DOI: 10.1159/000130330. View

5.
Muller H, Klinger H, Glasser M . Chromosome polymorphism in a human newborn population. II. Potentials of polymorphic chromosome variants for characterizing the idiogram of an individual. Cytogenet Cell Genet. 1975; 15(4):239-55. DOI: 10.1159/000130522. View