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PMID: 4443988 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

21 monosomy in a retarded female infant.

Journal of medical genetics ·Vol. 11 ·No. 4 ·1974-12-00 ·Pages 386-9

Halloran KH, Breg WR, Mahoney MJ

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Aneuploidy Chromosomes, Human, 21-22 and Y Female Heart Defects, Congenital Humans Hypertelorism/genetics Infant Intellectual Disability/genetics Karyotyping Micrognathism/genetics

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Halloran K H

Breg W R

Mahoney M J

References (8)

8 references, click to expand

Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
Cytogenetics. 1971;10(6):413-26 PMID: 5146418
A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype.
J Med Genet. 1972 Mar;9(1):110-5 PMID: 5025474
Chromosome banding with acridine orange.
Lancet. 1972 Dec 16;2(7790):1311 PMID: 4117838
An 18p21q translocation in a patient with presumptive "monosomy G".
Am J Dis Child. 1972 Dec;124(6):908-10 PMID: 4639227
A "G" deletion syndrome anti-mongolism.
Acta Paediatr Scand. 1973 Mar;62(2):216-20 PMID: 4691464
An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques.
Ann Genet. 1973 Mar;16(1):11-6 PMID: 4124663
Monosomy of a "G" autosome in a 22-year-old female.
Med J Aust. 1973 Jul 28;2(4):178-80 PMID: 4741347
Monosomy of chromosome No. 22. A case report.
J Pediatr. 1973 Nov;83(5):836-8 PMID: 4126387

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

10.1136/jmg.11.4.386

Published

1974-12-00

Pages

386-9

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1013214

Subset

External Links

PubMed source DOI: 10.1136/jmg.11.4.386 PMC Full Text View journal details

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21 monosomy in a retarded female infant.

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