Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

Humangenetik ·Vol. 12 ·No. 3 ·1971-00-00 ·Pages 175-81

Hoehn H, Engel W, Reinwein H

Abstract

暂无摘要

MeSH Terms

Cell Division Chromosome Aberrations Chromosomes, Human, 6-12 and X Dermatoglyphics Humans Infant Intellectual Disability/genetics Karyotyping Male Trisomy

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Hoehn H

Engel W

Reinwein H

References (7)

7 references, click to expand

Satellite DNA associated with heterochromatin in Rhynchosciara.
Chromosoma. 1971 Mar 16;32(4):407-27 PMID: 4102329
[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
Ann Genet. 1970 Dec;13(4):217-32 PMID: 5313386
Deletions of the X chromosomes in Microtus agrestis cells in vitro.
Cytogenetics. 1970;9(6):468-84 PMID: 5519129
Familial transmission of an unusual variant of a group C chromosome.
Ann Genet. 1970 Sep;13(3):183-6 PMID: 5313145
Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9.
Humangenetik. 1969;7(1):22-7 PMID: 4238957
Preferential breakage of sensitive regions of human chromosomes.
Humangenetik. 1970;8(4):295-301 PMID: 4245032
[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

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00702772

Published

1971-00-00

Pages

175-81

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00702772

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Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

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