Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.

Human genetics ·Vol. 52 ·No. 2 ·1979-11-00 ·Pages 175-8

Sandig KR, Mücke J, Veit H

Abstract

Trisomy 9p with de novo 9/15 translocation and 9p isochromosome was observed in a mentally defective boy with typical clinical features for this syndrome. This chromosomal aberration is probably caused by the pericentric inversion of chromosome 9 of the patient's father.

MeSH Terms

Child, Preschool Chromosome Banding Chromosomes, Human, 13-15 Chromosomes, Human, 6-12 and X Female Humans Intellectual Disability/genetics Karyotyping Male Pedigree Translocation, Genetic Trisomy

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Sandig K R

Mücke J

Veit H

References (10)

10 references, click to expand

Trisomy 9p with an isochromosome of 9p.
Hum Genet. 1978 May 16;42(1):93-7 PMID: 649175
A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
Clin Genet. 1975 Feb;7(2):134-43 PMID: 1132161
[Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations (author's transl)].
Humangenetik. 1973 Dec 10;20(3):273-82 PMID: 4772080
Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
Humangenetik. 1971;12(3):175-81 PMID: 5563410
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
Humangenetik. 1973 Apr 16;18(2):129-38 PMID: 4124236
A presumptive tetrasomy for the short arm of chromosome 9.
Humangenetik. 1974;25(3):163-70 PMID: 4141333
Genetics of the +p9 syndrome.
Hum Genet. 1976 Apr 15;32(1):23-33 PMID: 770307
Structural variability of human chromosome 9 in relation to its evolution.
Hum Genet. 1976 Mar 12;31(3):247-62 PMID: 955624
A case of trisomy for the short arm of chromosome no. 9(+9(p)).
Hum Genet. 1976 Sep 10;34(1):77-80 PMID: 965010
[Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].
Ann Genet. 1966;9(1):12-8 PMID: 5295698

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

10.1007/BF00271570

Published

1979-11-00

Pages

175-8

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

PubMed source DOI: 10.1007/BF00271570 View journal details

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Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.

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