Literature DB >> 7428770

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

J P Fryns, J C Pedersen, H Duyck, G Fabry, H Van den Berghe.   

Abstract

A partial deletion of the short arm of chromosome 9 is reported in a female newborn and a 12.5 year-old male. The features expressed by both patients, and especially the peculiar type of the craniofacial dysmorphism, confirm the existence of a typical clinical syndrome associated with this partial autosomal monosomy.

Entities:  

Mesh：

Year:  1980        PMID： 7428770     DOI： 10.1007/bf00441473

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


  14 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.  Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870.

Authors:  W R Breg; M M Aronson; R Hill; A E Greene; L L Coriell
Journal:  Cytogenet Cell Genet       Date:  1976

3.  A case of 9p- syndrome.

Authors:  Y Kuroki; S Yokota; H Nakai; Y Yamamoto; I Matsui
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

4.  The 9p--syndrome.

Authors:  O S Alfi; G N Donnell; A Derencsenyi
Journal:  Birth Defects Orig Artic Ser       Date:  1976

5.  The deletion 9p syndrome. A 61-year-old man with deletion of short arm 9.

Authors:  J Nielsen; A Homma; F Christiansen; K Rasmussen; P Saldaña-Garcia
Journal:  Clin Genet       Date:  1977-08       Impact factor: 4.438

6.  A case of partial 9p monosomy with some unusual clinical features.

Authors:  F J Rutten; T W Hustinx; A A Dunk-Tillemans; J M Scheres; Y S Tjon
Journal:  Ann Genet       Date:  1978-03

7.  Another case of 9P-syndrome.

Authors:  M T Mulcahy
Journal:  Ann Genet       Date:  1978-03

8.  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

9.  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

10.  The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction.

Authors:  F Bergamo; F Crosato; D Francesconi; F Pasqual; O Zuffardi
Journal:  Clin Genet       Date:  1977-03       Impact factor: 4.438
View more
  2 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.  A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42.

Authors:  Ali Vahabi; Filiz Hazan; Isa Abdi Rad
Journal:  Maedica (Bucur)       Date:  2017-01
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.