Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.

Humangenetik ·Vol. 1 ·No. 5 ·1965-00-00 ·Pages 479-82

Hirschhorn K, Cooper HL, Firschein IL

Abstract

暂无摘要

MeSH Terms

Child, Preschool Chromosome Aberrations Chromosome Disorders Cri-du-Chat Syndrome Dermatoglyphics Humans Jaw Abnormalities

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Hirschhorn K

Cooper H L

Firschein I L

References (3)

3 references, click to expand

[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
C R Hebd Seances Acad Sci. 1963 Nov 18;257:3098-102 PMID: 14095841
CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.
Cytogenetics. 1964;3:347-52 PMID: 14248464
[Deficiency on the short arms of a chromosome No. 4].
Humangenetik. 1965;1(5):397-413 PMID: 5868696

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

Published

1965-00-00

Pages

479-82

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

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