Literature DB >> 308342

Another case of 9P-syndrome.

M T Mulcahy.   

Abstract

This paper discusses the value of an International Repository of Chromosomal Abnormalities and Variants as a means of communication and case finding. A further case of 9p- is described. The clinical and cytogenetic findings confirm the existence of a clinical entity which in many respects is the opposite of the 9p trisomy syndrome.

Entities:  

Mesh：

Year:  1978        PMID： 308342

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  3 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.  Where is the gene for GALT?

Authors:  M T Mulcahy; R G Wilson
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

3.  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
  3 in total

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