A case of partial trisomy 3q.

Journal of medical genetics ·Vol. 13 ·No. 6 ·1976-12-00 ·Pages 525-8

Chiyo H, Kuroki Y, Matsui I, Niitsu N, Nakogome Y

Abstract

暂无摘要

MeSH Terms

Chromosome Aberrations Chromosome Disorders Chromosomes, Human, 1-3 Female Humans Infant, Newborn Trisomy

Authors & Affiliations

5 authors, click to expand affiliations / ORCID

Chiyo H

Kuroki Y

Matsui I

Niitsu N

Nakogome Y

References (5)

5 references, click to expand

An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12.
J Med Genet. 1974 Sep;11(3):303-5 PMID: 4139264
A new translocation syndrome (3/B).
N Engl J Med. 1966 Aug 11;275(6):290-8 PMID: 4957370
A familial 3-18 reciprocal translocation resulting in chromosome duplication-deficiency (3?plus-18q minus).
Acta Paediatr Scand. 1969 Jul;58(4):397-406 PMID: 4186441
[Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)].
Ann Genet. 1972 Sep;15(3):159-65 PMID: 4539763
Presumptive trisomy for human chromosome number 3.
Acta Genet Stat Med. 1968;18(6):584-92 PMID: 5756531

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

Published

1976-12-00

Pages

525-8

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1013486

Subset

External Links

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