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Journal Abstract Search
163 related items for PubMed ID: 890108
1. Are the acrocephalosyndactyly syndromes variable expressions of a single gene defect? Escobar V, Bixler D. Birth Defects Orig Artic Ser; 1977; 13(3C):139-54. PubMed ID: 890108 [Abstract] [Full Text] [Related]
2. On the classification of the acrocephalosyndactyly syndromes. Escobar V, Bixler D. Clin Genet; 1977 Sep; 12(3):169-78. PubMed ID: 908170 [Abstract] [Full Text] [Related]
3. Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations. Ito S, Sekido K, Kanno H, Sato H, Tanaka M, Yamaguchi K, Yamamoto I. J Neurosurg; 2005 Jan; 102(1 Suppl):23-30. PubMed ID: 16206730 [Abstract] [Full Text] [Related]