Multiple congenital defects associated with trisomy for the short arm of chromosome 4.

Journal of medical genetics ·Vol. 11 ·No. 3 ·1974-09-00 ·Pages 291-5

Owen L, Martin B, Blank CE, Harris F

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Adult Anus, Imperforate/genetics Chromosomes, Human, 21-22 and Y Chromosomes, Human, 4-5 Dermatoglyphics Face Female Humans Infant, Newborn Karyotyping Lymphocytes/ultrastructure Male Microphthalmos/genetics Syndrome Translocation, Genetic Trisomy

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Owen L

Martin B

Blank C E

Harris F

References (7)

7 references, click to expand

[The crying cat syndrome and its reciprocal].
Ann Genet. 1965;8(1):11-5 PMID: 5294630
[Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].
Ann Genet. 1966 Sep;9(3):113-22 PMID: 5298289
Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.
Am J Hum Genet. 1967 Jul;19(4):586-603 PMID: 6036276
[Segregation of a balanced translocation t(5p-;Gp+)].
Ann Genet. 1968 Dec;11(4):247-52 PMID: 5306368
A rapid banding technique for human chromosomes.
Lancet. 1971 Oct 30;2(7731):971-2 PMID: 4107917
[Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].
Humangenetik. 1972;15(2):163-71 PMID: 5049069
A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.
Acta Paediatr. 1964 Mar;53:172-81 PMID: 14128177

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

10.1136/jmg.11.3.291

Published

1974-09-00

Pages

291-5

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1013146

Subset

External Links

PubMed source DOI: 10.1136/jmg.11.3.291 PMC Full Text View journal details

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Multiple congenital defects associated with trisomy for the short arm of chromosome 4.

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