| Literature DB >> 7472832 |
I R Rivera-Matos1, R M Rakita, M M Mariscalco, F F Elder, S A Dreyer, T G Cleary.
Abstract
An infant had clinical signs suggestive of Hirschsprung disease as the initial manifestation of leukocyte adhesion deficiency. Chromosome studies showed a deletion of the distal third of the long arm of one chromosome 21, and flow cytometric studies confirmed the defective expression of CD18.Entities:
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Year: 1995 PMID： 7472832 DOI： 10.1016/s0022-3476(95)70169-9
Source DB: PubMed Journal: J Pediatr ISSN： 0022-3476 Impact factor: 4.406