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Journal Abstract Search
402 related items for PubMed ID: 20728324
1. [Adams-Oliver syndrome: a case with minimal expression]. Messerer M, Diabira S, Belliard H, Hamlat A. Arch Pediatr; 2010 Oct; 17(10):1460-4. PubMed ID: 20728324 [Abstract] [Full Text] [Related]
5. Autosomal dominant aplasia cutis in three generations and one case with preaxial polydactyly in the last generation. Yağci-Küpeli B, Çağlar K, Büyük S, Balci S. Genet Couns; 2011 May; 22(1):55-61. PubMed ID: 21614989 [Abstract] [Full Text] [Related]
8. Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations. Jones KM, Silfvast-Kaiser A, Leake DR, Diaz LZ, Levy ML. Pediatr Dermatol; 2017 Sep; 34(5):e249-e253. PubMed ID: 28884918 [Abstract] [Full Text] [Related]