A new case of partial trisomy 15q-.

Human genetics ·Vol. 51 ·No. 3 ·1979-10-02 ·Pages 335-8

Geneix A, Jaffray JY, Malet P, Foulon E, Jalbert P, Crost P

Abstract

Partial trisomy 15 was observed in a newborn with malformations of the head and extremities. A t(5;15) translocation was found in the mother and maternal grandfather.

MeSH Terms

Abnormalities, Multiple/genetics Adult Child Chromosome Banding Chromosomes, Human, 16-18 Female Humans Infant, Newborn Karyotyping Male Pedigree Translocation, Genetic Trisomy

Authors & Affiliations

6 authors, click to expand affiliations / ORCID

Geneix A

Jaffray J Y

Malet P

Foulon E

Jalbert P

Crost P

References (6)

6 references, click to expand

A case of partial trisomy 15.
J Med Genet. 1974 Dec;11(4):400-2 PMID: 4443991
[A new technic of analysis of the human karyotype].
C R Acad Sci Hebd Seances Acad Sci D. 1971 May 17;272(20):2638-40 PMID: 4104656
A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange.
J Pediatr. 1975 Jun;86(6):916-7 PMID: 1127534
An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
Ann Genet. 1975 Jun;18(2):99-103 PMID: 1081372
Familial partial trisomy 15.
Ann Genet. 1977 Sep;20(3):159-65 PMID: 304698
Human gene mapping using an X/autosome translocation.
Somatic Cell Genet. 1976 Mar;2(2):125-40 PMID: 69325

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

10.1007/BF00283405

Published

1979-10-02

Pages

335-8

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

PubMed source DOI: 10.1007/BF00283405 View journal details

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A new case of partial trisomy 15q-.

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