Literature DB >> 1218215

10p-: a new autosomal deletion syndrome?

U Francke, G M Mahan, B K Dixson, O W Jones.   

Abstract

Mesh:

Year:  1975        PMID: 1218215

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


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  1 in total

1.  Partial monosomy 10p syndrome.

Authors:  J M Klep-de Pater; J B Bijlsma; F M Alkema
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

  1 in total

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