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PMID: 1017321 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870.

Cytogenetics and cell genetics ·Vol. 17 ·No. 5 ·1976-00-00 ·Pages 296-7

Breg WR, Aronson MM, Hill R, Greene AE, Coriell LL

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Adult Chromosome Aberrations Chromosome Deletion Chromosomes, Human, 13-15 Chromosomes, Human, 6-12 and X Female Humans Microcephaly/genetics

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Breg W R

Aronson M M

Hill R

Greene A E

Coriell L L

Article Info

Journal

Cytogenetics and cell genetics

Abbr.

Cytogenet Cell Genet

ISSN

0301-0171

DOI

10.1159/000130726

Published

1976-00-00

Pages

296-7

Language

English

Region

Switzerland

NLM ID

0367735

Subset

External Links

PubMed source DOI: 10.1159/000130726

Analysis Services

Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870.

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