Langer-Giedion syndrome and deletion of the long arm of chromosome 8.

Human genetics ·Vol. 58 ·No. 2 ·1981-00-00 ·Pages 231-2

Fryns JP, Logghe N, van Eygen M, Van den Berghe H

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Child, Preschool Chromosome Deletion Chromosomes, Human, 6-12 and X Exostoses, Multiple Hereditary/genetics Fingers/abnormalities Hair/abnormalities Humans Male Nose/abnormalities Syndrome

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Fryns J P

Logghe N

van Eygen M

Van den Berghe H

References (3)

3 references, click to expand

Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21).
Hum Genet. 1979 Apr 17;48(1):127-30 PMID: 457127
Langer-Giedion syndrome and additional congenital malformations with interstitial deletion of the long arm of chromosome 8 46, XY, del 8 (q 13-22).
Clin Genet. 1980 Aug;18(2):142-6 PMID: 6254701
Chromosome deletion and multiple cartilaginous exostoses.
Eur J Pediatr. 1980 Mar;133(2):163-6 PMID: 6965910

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

10.1007/BF00278720

Published

1981-00-00

Pages

231-2

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

PubMed source DOI: 10.1007/BF00278720 View journal details

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Langer-Giedion syndrome and deletion of the long arm of chromosome 8.

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