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PMID: 631856 Published · ppublish English Case Reports Comparative Study Journal Article

Trisomy 10p due to t(5;10)(p15;p11) segregating in a large sibship.

Human genetics ·Vol. 41 ·No. 1 ·1978-02-23 ·Pages 11-7

Back E, Vogel W, Hertel C, Schuchmann L

Abstract

A family is reported with a segregating t(5;10)(p15;p11) translocation resulting in a child carrying trisomy 10p. The clinical findings of the patient are compared with trisomy 10p and the Cri-du-Chat syndrome.

MeSH Terms
Abnormalities, Multiple/genetics Autopsy Chromosomes, Human, 6-12 and X Cri-du-Chat Syndrome/genetics Female Humans Infant, Newborn Karyotyping Pedigree Translocation, Genetic Trisomy
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Back E
Vogel W
Hertel C
Schuchmann L
References (14)
14 references, click to expand
  1. [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].
    Ann Genet. 1976 Sep;19(3):195-7 PMID: 1086628
  2. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
    Ann Genet. 1975 Mar;18(1):5-11 PMID: 1080038
  3. Differences in DNA composition along mammalian metaphase chromosomes.
    Chromosoma. 1973 Jul 18;42(4):365-82 PMID: 4730556
  4. Trisomy for the short arm of chromosome No. 10.
    Clin Genet. 1974;6(5):408-15 PMID: 4434655
  5. Localization of the deleted segment in the Cri-du-Chat syndrome.
    Humangenetik. 1972;16(4):357-8 PMID: 4641843
  6. Partial trisomy 10p.
    Humangenetik. 1975 Sep 10;29(2):141-4 PMID: 1176136
  7. [A case of multiple congenital anomalies with familial C-G translocation].
    Jinrui Idengaku Zasshi. 1970 Mar;14(4):309-15 PMID: 5464693
  8. Partial trisomy 10p and familial translocation t(7;10)(p22;p12).
    Hum Genet. 1977 Mar 14;35(3):353-6 PMID: 844878
  9. Trisomy of the short arm of chromosome 10.
    J Med Genet. 1975 Dec;12(4):412-4 PMID: 1219122
  10. Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.
    Humangenetik. 1971;12(1):67-73 PMID: 4104181
  11. Trisomy iop.
    Ann Genet. 1976 Mar;19(1):57-60 PMID: 1084124
  12. Brother and sister with trisomy 10p: a new syndrome.
    Humangenetik. 1974;23(3):163-72 PMID: 4844639
  13. [Trisomy 10 p. A previously reported case explained by binding].
    Ann Genet. 1976 Mar;19(1):61-4 PMID: 1084125
  14. An intersexual infant with an extra chromosome.
    Ann Genet. 1968 Jun;11(2):88-94 PMID: 5303428
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
DOI
10.1007/BF00278867
Published
1978-02-23
Pages
11-7
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00278867 View journal details
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