Identification of a familial 19-21 translocation by Q and G band patterns.

Humangenetik ·Vol. 18 ·No. 3 ·1973-05-25 ·Pages 219-24

Vogel W, Löning B

Abstract

暂无摘要

MeSH Terms

Adult Cells, Cultured Child Chromosome Aberrations Chromosomes, Human, 19-20 Chromosomes, Human, 21-22 and Y Female Humans Infant Karyotyping Lymphocytes Male Meiosis Middle Aged Mitosis Pedigree Trisomy

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Vogel W

Löning B

References (7)

7 references, click to expand

Maternal transmission of a 21/1 translocation associated with Down's syndrome.
J Pediatr. 1966 Oct;69(4):635-9 PMID: 4224157
Ring formation of chromosomes nos. 19 and 20.
Cytogenetics. 1972;11(3):208-15 PMID: 5038363
Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.
Am J Hum Genet. 1972 Mar;24(2):189-213 PMID: 5016511
A simplified method of demonstrating Giemsa-band pattern in human chromosomes.
Humangenetik. 1971;14(1):83-4 PMID: 5144910
Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.
Humangenetik. 1971;12(1):67-73 PMID: 4104181
Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.
Clin Genet. 1972;3(4):226-48 PMID: 4262353
[Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].
Ann Genet. 1966;9(1):12-8 PMID: 5295698

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00290600

Published

1973-05-25

Pages

219-24

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00290600

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Identification of a familial 19-21 translocation by Q and G band patterns.

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