Familial short arm deletion of chromosome no. 15.

Humangenetik ·Vol. 21 ·No. 3 ·1974-00-00 ·Pages 283-6

Hoo JJ, Hillig U, Cramer H, Hansen S, Hermann F

Abstract

暂无摘要

MeSH Terms

Adolescent Adult Anorexia Nervosa/genetics Chromosome Aberrations Chromosomes, Human, 13-15 Female Humans Karyotyping Male Pedigree Phenotype Staining and Labeling

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Hoo J J

Hillig U

Cramer H

Hansen S

Hermann F

References (9)

9 references, click to expand

Exclusion of marker genes from the short arm of the human chromosome D1 by deletion mapping.
Hereditas. 1969;62(1):116-30 PMID: 5399209
Haptoglobin: a locus on the D1 chromosome?
Am J Hum Genet. 1967 May;19(3 Pt 2):393-8 PMID: 6026932
Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.
Clin Pediatr (Phila). 1969 Aug;8(8):453-8 PMID: 5797429
Atypical acrocentric chromosomes in Negro and Caucasian Mongols.
Am J Hum Genet. 1967 Mar;19(2):162-73 PMID: 4225661
Chromosome studies on randomly chosen men and women.
Lancet. 1965 Sep 18;2(7412):561-2 PMID: 4158190
[A short arm deletion of chromosome 13].
Ann Genet. 1968 Sep;11(3):184-6 PMID: 5304619
FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS.
Bull Johns Hopkins Hosp. 1965 Jun;116:396-402 PMID: 14300779
[Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family].
Ann Genet. 1966 Jun;9(2):80-5 PMID: 5296303
Short arm deletion of chromosome 14.
Humangenetik. 1972;15(1):33-8 PMID: 5046906

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00279024

Published

1974-00-00

Pages

283-6

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00279024

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Familial short arm deletion of chromosome no. 15.

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