Literature DB >> 903150

A case of 9p- syndrome.

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

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.

Entities:  

Mesh：

Year:  1977        PMID： 903150     DOI： 10.1007/bf00295813

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  9 in total

1.  [Partial deletion of the short arm of the chromosome 9].

Authors:  F Serville; D Allain; A Broustet; C Martin; M Gachet; J P Babin; J Cenraud
Journal:  Ann Genet       Date:  1976-06

2.  The 9p- syndrome.

Authors:  O S Alfi; G N Donnell; P W Allderdice; A Derencsenyi
Journal:  Ann Genet       Date:  1976-03

3.  The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation.

Authors:  E Orye; H Verhaaren; A M Van den Bogaert-Van Heesvelde
Journal:  Clin Genet       Date:  1975-11       Impact factor: 4.438

4.  A ring 9 chromosome. Repository identification no. GM-166.

Authors:  M L Kistenmacher; H H Punnett; M Aronson; R C Miller; A E Greene; L L Coriell
Journal:  Cytogenet Cell Genet       Date:  1975

5.  Mental retardation and congenital malformations associated with a ring chromosome 9.

Authors:  S Nakajima; M Yanagisawa; S Kamoshita; Y Nakagome
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

6.  [A case of annular chromosome 9. Indentification by controlled denaturation].

Authors:  J Fraisse; B Lauras; M J Ooghe; F Freycon; M O Rethoré
Journal:  Ann Genet       Date:  1974-09

7.  Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.

Authors:  O Alfi; G N Donnell; B F Crandall; A Derencsenyi; R Menon
Journal:  Ann Genet       Date:  1973-03

8.  A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.

Authors:  P Jacobsen; M Mikkelsen; F Rosleff
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

9.  Comparative behavior of ring chromosomes.

Authors:  M L Kistenmacher; H H Punnett
Journal:  Am J Hum Genet       Date:  1970-05       Impact factor: 11.025
  9 in total
  6 in total

Review 1.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

2.  The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes.

Authors:  R S Young; T Reed; M E Hodes; C G Palmer
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Partial monosomy of the short arm of chromosome 9: a distinct clinical entity.

Authors:  J Deroover; J P Fryns; C Parloir; J Haegeman; H van den Berghe
Journal:  Hum Genet       Date:  1978-10-31       Impact factor: 4.132

4.  Deletion of the short arm of chromosome 9. A clinically recognisable entity.

Authors:  J P Fryns; J C Pedersen; H Duyck; G Fabry; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1980-09       Impact factor: 3.183

5.  The 9p-syndrome.

Authors:  S J Funderburk; R S Sparkes; I Klisak
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

6.  Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations.

Authors:  Nirmala D Sirisena; U Kalpani S Wijetunge; Ramya de Silva; Vajira H W Dissanayake
Journal:  Case Rep Genet       Date:  2013-07-25
  6 in total

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