Trisomy 4p due to a paternal t(4p-;16p+) translocation.

Human genetics ·Vol. 34 ·No. 2 ·1976-10-28 ·Pages 227-30

Bauknecht T, Betteken F, Vogel W

Abstract

A patient is described carrying a duplication 4p12 leads to pter due to a paternal translocation: 46,XY,t(4;16) (p12;p13). Involvement of chromosome No. 16 and the heterogeneity of the clinical picture in cases with dup (4p) are discussed.

MeSH Terms

Chromosome Aberrations Chromosomes, Human, 16-18 Chromosomes, Human, 4-5 Humans Male Pedigree Phenotype Translocation, Genetic Trisomy

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Bauknecht T

Betteken F

Vogel W

References (6)

6 references, click to expand

Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.
Humangenetik. 1975 Oct 7;29(4):329-35 PMID: 1176148
Localization of heterochromatin in human chromosomes.
Cytogenetics. 1971;10(2):81-6 PMID: 4106483
Differences in DNA composition along mammalian metaphase chromosomes.
Chromosoma. 1973 Jul 18;42(4):365-82 PMID: 4730556
A family with an inherited translocation involving the no. 4/no. 21 chromosomes.
J Med Genet. 1975 Dec;12(4):408-11 PMID: 1219121
Identification of human chromosomes by DNA-binding fluorescent agents.
Chromosoma. 1970;30(2):215-27 PMID: 4193398
[Trisomy 4p. Three new observations (author's transl)].
Humangenetik. 1975 Nov 6;30(2):99-108 PMID: 1193607

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

10.1007/BF00278894

Published

1976-10-28

Pages

227-30

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

PubMed source DOI: 10.1007/BF00278894 View journal details

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Trisomy 4p due to a paternal t(4p-;16p+) translocation.

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