A familial reciprocal translocation between three chromosomes.

Humangenetik ·Vol. 24 ·No. 4 ·1974-00-00 ·Pages 303-8

Creasy MR, Crolla JA, Daker MG

Abstract

暂无摘要

MeSH Terms

Abortion, Spontaneous/genetics Adult Chromosome Aberrations Chromosomes, Human, 1-3 Chromosomes, Human, 13-15 Chromosomes, Human, 4-5 Embryo, Mammalian/ultrastructure Female Heterozygote Humans Karyotyping Male Meiosis Pedigree Pregnancy Recombination, Genetic Staining and Labeling Translocation, Genetic

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Creasy M R

Crolla J A

Daker M G

References (7)

7 references, click to expand

A rapid banding technique for human chromosomes.
Lancet. 1971 Oct 30;2(7731):971-2 PMID: 4107917
A complex familial translocation involving chromosomes 5, 9 and 13.
Cytogenetics. 1970;9(4):294-306 PMID: 5474810
Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
Humangenetik. 1974 Apr 24;22(1):59-65 PMID: 4134840
An analysis of the break points of structural rearrangements in man.
J Med Genet. 1974 Mar;11(1):50-64 PMID: 4134839
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.
Humangenetik. 1971;13(3):205-9 PMID: 5114675
A case of multople chromosomal rearrangements with persistence of foetal haemoglobin.
Cytogenetics. 1968;7(3):169-82 PMID: 5682897
Localization of heterochromatin in human chromosomes.
Cytogenetics. 1971;10(2):81-6 PMID: 4106483

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00297594

Published

1974-00-00

Pages

303-8

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00297594

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A familial reciprocal translocation between three chromosomes.

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