Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.

Journal of medical genetics ·Vol. 11 ·No. 3 ·1974-09-00 ·Pages 299-303

Hobolth N, Jacobsen P, Mikkelsen M

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Adult Chromosome Aberrations Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Face Female Humans Infant Intellectual Disability/genetics Karyotyping Male Microscopy, Fluorescence Pedigree Staining and Labeling Translocation, Genetic Trisomy

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Hobolth N

Jacobsen P

Mikkelsen M

References (5)

5 references, click to expand

Identification of human chromosomes by DNA-binding fluorescent agents.
Chromosoma. 1970;30(2):215-27 PMID: 4193398
Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.
Am J Hum Genet. 1972 Mar;24(2):189-213 PMID: 5016511
[Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation].
Ann Genet. 1972 Dec;15(4):283-6 PMID: 4539489
Identification of partial 12 trisomy by quinacrine fluorescence.
J Pediatr. 1973 Feb;82(2):269-72 PMID: 4119313
[Familial case of t(3q-; 12q+) translocation].
Ann Genet. 1973 Jun;16(2):131-4 PMID: 4541906

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

10.1136/jmg.11.3.299

Published

1974-09-00

Pages

299-303

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1013149

Subset

External Links

PubMed source DOI: 10.1136/jmg.11.3.299 PMC Full Text View journal details

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Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.

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