Literature DB >> 1684352

De novo deletion of chromosome 9 (9p-) in a child with multiple congenital anomalies and psychomotor retardation.

D S Murthy1, S K Murthy, G J Banker, A J Patel.   

Abstract

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Year:  1991        PMID： 1684352

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN： 0019-6061            Impact factor:   1.411


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  1 in total

1.  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
  1 in total

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