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pro vyhledávání: '"M. L. C. Moreira"'
Publikováno v:
Genetics and molecular research : GMR. 13(2)
We report two similarly affected cousins (children of monozygotic twin sisters) with phenotypic features consistent with 9p deletion syndrome, including dysmorphic craniofacial features (trigonocephaly, midface hypoplasia, upward-slanting palpebral f