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PMID: 903150 Published · ppublish English Case Reports Journal Article

A case of 9p- syndrome.

Human genetics ·Vol. 38 ·No. 1 ·1977-08-31 ·Pages 107-11

Kuroki Y, Yokota S, Nakai H, Yamamoto Y, Matsui I

Abstract

An 8-month-old female child with the 9p- karyotype: 46,XX,del(9) (p22) is presented, being the first case from among Oriental people. She has many clinical features similar to those described in Caucasian cases.

MeSH Terms
Chromosome Aberrations/genetics Chromosome Disorders Chromosomes, Human, 6-12 and X Dermatoglyphics Female Humans Infant Karyotyping Syndrome
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Kuroki Y
Yokota S
Nakai H
Yamamoto Y
Matsui I
References (9)
9 references, click to expand
  1. Comparative behavior of ring chromosomes.
    Am J Hum Genet. 1970 May;22(3):304-18 PMID: 5445002
  2. A ring 9 chromosome. Repository identification no. GM-166.
    Cytogenet Cell Genet. 1975;15(2):122-3 PMID: 1183236
  3. Mental retardation and congenital malformations associated with a ring chromosome 9.
    Hum Genet. 1976 Jun 29;32(3):289-93 PMID: 939548
  4. [Partial deletion of the short arm of the chromosome 9].
    Ann Genet. 1976 Jun;19(2):143 PMID: 1085605
  5. Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.
    Ann Genet. 1973 Mar;16(1):17-22 PMID: 4541805
  6. The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation.
    Clin Genet. 1975 Nov;8(5):349-57 PMID: 1204232
  7. [A case of annular chromosome 9. Indentification by controlled denaturation].
    Ann Genet. 1974 Sep;17(3):175-80 PMID: 4548818
  8. The 9p- syndrome.
    Ann Genet. 1976 Mar;19(1):11-6 PMID: 1084115
  9. A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
    Clin Genet. 1973;4(5):434-41 PMID: 4127395
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
DOI
10.1007/BF00295813
Published
1977-08-31
Pages
107-11
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00295813 View journal details
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