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PMID: 944684 Published · ppublish English Case Reports Journal Article

Trisomy 9p resulting from maternal 9/21 translocation.

Human genetics ·Vol. 32 ·No. 2 ·1976-05-19 ·Pages 217-20

Sŭbrt I, Blehová B, Pallová B

Abstract

The clinical picture found in a child with trisomy 9p confirmed that this chromosomal syndrome is a entity, which arises from maternal translocation t(9;21).

MeSH Terms
Abnormalities, Multiple/genetics Chromosome Aberrations Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Dermatoglyphics Female Humans Infant Infant, Newborn Infant, Premature Karyotyping Translocation, Genetic Trisomy
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sŭbrt I
Blehová B
Pallová B
References (18)
18 references, click to expand
  1. A case of trisomy 9p in a family with translocation 9/15.
    Humangenetik. 1975;27(4):353-8 PMID: 1150257
  2. A new case of trisomy for the short arm of No. 9 chromosome.
    J Med Genet. 1973 Sep;10(3):296-9 PMID: 4774540
  3. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
    Clin Genet. 1975 Feb;7(2):134-43 PMID: 1132161
  4. [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
  5. [Trisomy 9p : 2 further cases].
    Ann Genet. 1974 Sep;17(3):167-74 PMID: 4548817
  6. [Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].
    Z Kinderheilkd. 1971;109(4):293-9 PMID: 5555168
  7. Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.
    Humangenetik. 1971;12(3):175-81 PMID: 5563410
  8. Partial trisomy 9 in the case of familial translocation 8/9 mat.
    Ann Genet. 1974 Sep;17(3):163-6 PMID: 4548816
  9. [Trisomy 9p gy t(4; 9) (q 34; q21) mat].
    Ann Genet. 1974 Sep;17(3):157-61 PMID: 4548815
  10. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
    J Pediatr. 1974 Jul;85(1):92-5 PMID: 4855265
  11. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Humangenetik. 1973 Apr 16;18(2):129-38 PMID: 4124236
  12. A new translocation between chromosomes in the 6-12 and 21-22 groups.
    J Med Genet. 1967 Sep;4(3):169-76 PMID: 5583342
  13. [Cp trisomy: a new syndrome].
    Ann Genet. 1971 Sep;14(3):177-86 PMID: 5315464
  14. Trisomy 9p in a patient with a de novo 9/15 translocation.
    Clin Genet. 1975 Apr;7(4):317-24 PMID: 1126053
  15. Congenital anomalies due to transmission of a chromosome translocation.
    J Med Genet. 1966 Mar;3(1):59-61 PMID: 5911833
  16. [Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].
    Ann Genet. 1966;9(1):12-8 PMID: 5295698
  17. An intersexual infant with an extra chromosome.
    Ann Genet. 1968 Jun;11(2):88-94 PMID: 5303428
  18. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Ann Genet. 1969 Mar;12(1):15-27 PMID: 5306708
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
DOI
10.1007/BF00291508
Published
1976-05-19
Pages
217-20
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00291508 View journal details
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