Chromosome 1 heteromorphism in patients with malignant disease: a constitutional marker for a high-risk group?

British medical journal ·Vol. 1 ·No. 6057 ·1977-02-05 ·Pages 358

Atkin NB

Abstract

暂无摘要

MeSH Terms

Blood Cells/ultrastructure Chromosome Aberrations Chromosomes, Human, 1-3 Humans Lymphoid Tissue/ultrastructure Neoplasms/genetics,pathology Polymorphism, Genetic

Authors & Affiliations

1 authors, click to expand affiliations / ORCID

Atkin N B

References (5)

5 references, click to expand

Polymorphism of human C-band heterochromatin. I. Frequency of variants.
Am J Hum Genet. 1973 Mar;25(2):181-92 PMID: 4120239
A simple technique for demonstrating centromeric heterochromatin.
Exp Cell Res. 1972 Nov;75(1):304-6 PMID: 4117921
Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over.
Am J Hum Genet. 1975 Mar;27(2):178-89 PMID: 47710
Attraction between centric heterochromatin of human chromosomes.
Cytogenet Cell Genet. 1975;15(2):66-80 PMID: 1183239
Human Q and C chromosomal variations: distribution and incidence.
Cytogenet Cell Genet. 1975;14(2):97-115 PMID: 1149498

Article Info

Journal

British medical journal

Abbr.

Br Med J

ISSN

0007-1447

DOI

10.1136/bmj.1.6057.358

Published

1977-02-05

Pages

358

Language

English

Region

England

NLM ID

0372673

PMCID

PMC1604525

Subset

External Links

PubMed source DOI: 10.1136/bmj.1.6057.358 PMC Full Text

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Chromosome 1 heteromorphism in patients with malignant disease: a constitutional marker for a high-risk group?

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