Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).

Humangenetik ·Vol. 27 ·No. 3 ·1975-00-00 ·Pages 269-74

Stoll C, Levy JM, Gardea A

Abstract

暂无摘要

MeSH Terms

Adult Chromosome Aberrations Chromosomes, Human, 13-15 Chromosomes, Human, 19-20 Chromosomes, Human, 6-12 and X Cytogenetics Dermatoglyphics Female Humans Infant Karyotyping Pedigree Translocation, Genetic Trisomy

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Stoll C

Levy J M

Gardea A

References (7)

7 references, click to expand

[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
[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
A case of trisomy 9.
J Med Genet. 1973 Jun;10(2):184-7 PMID: 4714588
Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
Humangenetik. 1971;12(3):175-81 PMID: 5563410
Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.
J Med Genet. 1973 Mar;10(1):65-9 PMID: 4697854
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
Humangenetik. 1973 Apr 16;18(2):129-38 PMID: 4124236
Trisomy 9 mosaicism with multiple congenital anomalies.
J Med Genet. 1973 Jun;10(2):180-4 PMID: 4714587

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00278358

Published

1975-00-00

Pages

269-74

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00278358

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Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).

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