Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

American journal of human genetics ·Vol. 25 ·No. 1 ·1973-01-00 ·Pages 77-81

Warren RJ, Rimoin DL, Summitt RL

Abstract

暂无摘要

MeSH Terms

Blepharoptosis/genetics Child Child, Preschool Chromosome Aberrations/genetics Chromosome Disorders Chromosomes, Human, 21-22 and Y Diagnosis, Differential Down Syndrome/genetics Female Humans Intellectual Disability/genetics Lymphocytes/cytology Male Microcephaly/genetics Microscopy, Fluorescence Phenotype Quinacrine Syndrome

Chemicals

Quinacrine

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Warren R J

Rimoin D L

Summitt R L

References (11)

11 references, click to expand

[Ring G-chromosome. Report of two cases and review of literature].
Humangenetik. 1971;12(2):142-55 PMID: 4254972
DNA-binding fluorochromes for the study of the organization of the metaphase nucleus.
Exp Cell Res. 1969 Nov;58(1):141-52 PMID: 5408613
G-group ring chromosome in a mentally subnormal girl.
J Ment Defic Res. 1971 Mar;15(1):61-72 PMID: 4253116
Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.
Ann Genet. 1971 Mar;14(1):7-12 PMID: 5314299
The G deletion syndromes.
J Pediatr. 1970 Oct;77(4):658-63 PMID: 5454712
[The Dr phenotype: a study of threee cases with a ring D chromosome].
Ann Genet. 1968 Jun;11(2):79-87 PMID: 5303427
Ring-G chromosome, a new G-deletion syndrome?
Am J Dis Child. 1968 Apr;115(4):489-93 PMID: 4296014
G-deletion syndrome II.
Humangenetik. 1972;14(2):164-6 PMID: 5026850
Identification of 21r and 22r chromosomes by quinacrine fluorescence.
Clin Genet. 1972;3(4):264-70 PMID: 5054320
[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].
C R Hebd Seances Acad Sci. 1964 Nov 30;259:4187-90 PMID: 14260664
Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis.
Exp Cell Res. 1970 Nov;63(1):240-3 PMID: 4250490

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

Published

1973-01-00

Pages

77-81

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC1762232

Subset

External Links

PubMed source PMC Full Text View journal details

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Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

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