Chromosome 17 has a real fragile site at p12.

Human genetics ·Vol. 61 ·No. 2 ·1982-00-00 ·Pages 177-9

Shabtai F, Klar D, Halbrecht I

Abstract

暂无摘要

MeSH Terms

Chromosome Banding Chromosome Fragile Sites Chromosome Fragility Chromosomes, Human, 16-18/ultrastructure Humans Karyotyping

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Shabtai F

Klar D

Halbrecht I

References (5)

5 references, click to expand

Significance of chromosome 17ps+ in three generations of a family.
J Med Genet. 1970 Jun;7(2):142-7 PMID: 5519600
Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.
Am J Hum Genet. 1979 Mar;31(2):125-35 PMID: 36752
Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13.
Hum Genet. 1981;57(2):217-9 PMID: 7194847
Clinical significance of the satellited short arm of human chromosome 17 (17ps +) : a rare heteromorphism?
Ann Genet. 1979;22(3):133-6 PMID: 316666
Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.
Am J Hum Genet. 1979 Mar;31(2):136-48 PMID: 453198

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

Published

1982-00-00

Pages

177-9

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

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