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PMID: 939560 Published · ppublish English Case Reports Journal Article

Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome.

Human genetics ·Vol. 33 ·No. 1 ·1976-07-07 ·Pages 73-6

Dallapiccola B, Bollea G, Mazzilli C, Gandini E

Abstract

A case of partial trisomy 9 is described in a mentally retarded and dysmorphic child, confirming that this chromosome unbalance results in a characteristic clinical entity. This trisomy arose through aberrant segregation of translocation chromosome during meiosis in the patient's mother, who is a balanced heterozygote for a complex translocation involving chromosomes 9, 21 and 22. The phenotypically normal sister of the proposition is also carrier of the same complex translocation.

MeSH Terms
Child Chromosome Aberrations Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Humans Male Pedigree Phenotype Translocation, Genetic Trisomy
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dallapiccola B
Bollea G
Mazzilli C
Gandini E
References (5)
5 references, click to expand
  1. [New system of chromosome banding: the T bands (author's transl)].
    Chromosoma. 1973 Apr 27;41(4):395-402 PMID: 4127019
  2. Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.
    Clin Genet. 1975 Apr;7(4):261-73 PMID: 1126048
  3. Observations on specific giemsa staining of the Y and on selective oil destaining of the chromosomes.
    Humangenetik. 1975;26(3):251-5 PMID: 48496
  4. Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.
    Humangenetik. 1974;25(2):83-92 PMID: 4140843
  5. Trisomy 9p in a patient with a de novo 9/15 translocation.
    Clin Genet. 1975 Apr;7(4):317-24 PMID: 1126053
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1976-07-07
Pages
73-6
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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