Balanced familial translocation t(5;19)(q12;p or q11) with phenotypical abnormalities in a girl.

Humangenetik ·Vol. 27 ·No. 3 ·1975-00-00 ·Pages 263-7

Stoll C, Levy JM, Champy M

Abstract

暂无摘要

MeSH Terms

Adolescent Carotid Arteries/abnormalities Child Chromosome Aberrations Chromosomes, Human, 19-20 Chromosomes, Human, 4-5 Chromosomes, Human, 6-12 and X Female Humans Karyotyping Phenotype Prognathism/genetics Translocation, Genetic Urinary Tract/abnormalities Vision Disorders/genetics

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Stoll C

Levy J M

Champy M

References (4)

4 references, click to expand

[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
Criminal patients with XYY sex-chromosome complement.
Lancet. 1966 Mar 12;1(7437):565-6 PMID: 4159988
Deletion of the long arms of the Y chromosome with normal male development and intelligence.
J Med Genet. 1974 Jun;11(2):208-11 PMID: 4841088
Ring chromosome 15:r(15). Identification by R banding.
Humangenetik. 1975;27(3):259-62 PMID: 50276

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00278357

Published

1975-00-00

Pages

263-7

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00278357

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Balanced familial translocation t(5;19)(q12;p or q11) with phenotypical abnormalities in a girl.

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