Literature DB >> 1017321

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

W R Breg, M M Aronson, R Hill, A E Greene, L L Coriell.   

Abstract

Mesh：

Year:  1976        PMID： 1017321     DOI： 10.1159/000130726

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  5 in total

1.  Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

Authors:  L A Christ; C A Crowe; M A Micale; J M Conroy; S Schwartz
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

Review 2.  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

3.  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

4.  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

5.  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 in total

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