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4. Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosum. Baranzini SE, del Rey G, Nigro N, Szijan I, Chamoles N, Cresto JC. Am J Med Genet; 1997 Jun 13; 70(3):216-21. PubMed ID: 9188656 [Abstract] [Full Text] [Related]
7. A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations. Seven M, Suyugül Z, Yüksel A, Geçkinli B, Hacihanefioğlu S, Cenani A. Turk J Pediatr; 1998 Jun 13; 40(4):593-601. PubMed ID: 10028871 [Abstract] [Full Text] [Related]
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