[Abnormal C group chromosome in several members of the same family].

Anomalie d'un chromosome du group C chez plusiers membres d'une même famille.

Humangenetik ·Vol. 6 ·No. 4 ·1968-00-00 ·Pages 326-34

Emerit I, Vernant P

Abstract

暂无摘要

MeSH Terms

Abnormalities, Multiple/genetics Adult Autoradiography Blood Group Antigens Child Child, Preschool Chromosome Aberrations Chromosome Disorders Chromosomes, Human, 6-12 and X Dermatoglyphics Female Humans Intellectual Disability Karyotyping Male Pedigree Thymidine Tritium

Chemicals

Blood Group Antigens Tritium Thymidine

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Emerit I

Vernant P

References (5)

5 references, click to expand

[On two familial cases of complex translocations].
Ann Genet. 1965;8(1):21-30 PMID: 5294577
[MICROTECHNIC FOR THE STUDY OF HUMAN CHROMOSOMES FROM A HUMAN LEUKOCYTE CULTURE].
Ann Genet. 1964;7:45 PMID: 14242108
Aneusomie de recombinaison: three further examples.
Am J Hum Genet. 1966 Sep;18(5):467-84 PMID: 5927289
Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease.
Ann Hum Genet. 1966 Jul;30(1):77-84 PMID: 4225589
[Translocation of a part of the long arms of chromosome 5 on the long arms of a D group chromosome (Bq-,Dq+) in a child and its mother].
Humangenetik. 1967;4(2):166-73 PMID: 6078180

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

Published

1968-00-00

Pages

326-34

Language

fre

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source

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[Abnormal C group chromosome in several members of the same family].

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