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4. [The problem of diagnosis and risk in cases of acrocephaly]. Predescu V; Christodorescu D Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1975; 20(3):229-36. PubMed ID: 1085470 [No Abstract] [Full Text] [Related]
5. On the classification of the acrocephalosyndactyly syndromes. Escobar V; Bixler D Clin Genet; 1977 Sep; 12(3):169-78. PubMed ID: 908170 [TBL] [Abstract][Full Text] [Related]
6. [Genetic aspects of craniofacial dysostoses: the Crouzon disease and the d'Apert-Crouzon disease]. Lemaitre A; Van Reck J Acta Stomatol Belg; 1976; 73(3):279-85. PubMed ID: 1071345 [No Abstract] [Full Text] [Related]
17. Depigmentation of hair, skin, and eyes associated with the Apert syndrome. Margolis S; Siegel IM; Choy A; Breinin GM Birth Defects Orig Artic Ser; 1978; 14(6B):341-60. PubMed ID: 728574 [No Abstract] [Full Text] [Related]
18. [Apert-Crouzon syndrome, (report of a case) (author's transl)]. Giannikas A; Katsatos I Odontiatriki; 1974; 7(1):17-23. PubMed ID: 4527275 [No Abstract] [Full Text] [Related]
19. Physical and oral characteristics of Crouzon syndrome, Apert syndrome, and Pierre Robin sequence. Horbelt CV Gen Dent; 2008; 56(2):132-4. PubMed ID: 18348368 [No Abstract] [Full Text] [Related]
20. [REMARKS ON ACROCEPHALOSYNDACTYLIA]. RASQUIN P Ann Otolaryngol Chir Cervicofac; 1964; 81():223-32. PubMed ID: 14157563 [No Abstract] [Full Text] [Related] [Next] [New Search]