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» Articles » PMID: 5295911

[On a Case of Partial Deletion of the Short Arm of Chromosome 18, Resulting in a Familial 18c-17 Translocation]

Overview
Journal Ann Genet
Publisher Elsevier
Specialty Genetics
Date 1966 Jan 1
PMID 5295911
Citations 9
Authors
J LeJeune
R Berger
M O Rethore
P Paolini
J BOISSE
P MOZZICONACCI
Affiliations
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Citing Articles

Deletion of short arm of a chromosome 18 (46, XX, 18 p-).

REINWEIN H, Ritter H, Wolf U Humangenetik. 1967; 5(1):72-3.

PMID: 5585063 DOI: 10.1007/BF00286215.

On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Bender K, Burckhardt K Humangenetik. 1970; 9(1):75-85.

PMID: 5488998 DOI: 10.1007/BF00696016.

Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.

Fischer P, Golob E, Friedrich F, KUNZE-MUHL E, DOLESCHEL W, AICHMAIR H J Med Genet. 1970; 7(1):91-8.

PMID: 5480972 PMC: 1468926. DOI: 10.1136/jmg.7.1.91.

[On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].

Bender K, Ritter H, Wolf U Humangenetik. 1967; 4(2):85-103.

PMID: 4865216 DOI: 10.1007/BF00291253.

Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

TONDURY G Humangenetik. 1973; 18(1):16-32.

PMID: 4578677 DOI: 10.1007/BF00279027.