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48. [An autopsy case of Smith-Lemli-Opitz syndrome]. Nagao M; Iwadate K; Zhang WD; Takahashi H; Yamada Y; Suzuki H; Takatori T Nihon Hoigaku Zasshi; 1994 Aug; 48(4):274-8. PubMed ID: 7967168 [TBL] [Abstract][Full Text] [Related]
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50. Histopathology of the temporal bones in mandibulofacial dysostosis (Treacher-Collins syndrome). Sando I; Hemenway WG; Morgan WR Trans Am Acad Ophthalmol Otolaryngol; 1968; 72(6):913-24. PubMed ID: 5303735 [No Abstract] [Full Text] [Related]
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52. [On the pathogenesis and classification of mandibulo-facial dysplasias]. Eschler J Dtsch Med Wochenschr; 1965 Oct; 90(42):1873-80. PubMed ID: 4953259 [No Abstract] [Full Text] [Related]
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54. [Franceschetti-Zwahlen syndrome in a newborn infant]. Jabłońska-Ulbrych A; Przybylska T; Skomra S Pediatr Pol; 1980 Jan; 55(1):91-4. PubMed ID: 7367072 [No Abstract] [Full Text] [Related]
55. Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second family. Wulfsberg EA; Campbell AB; Lurie IW; Eanet KR Am J Med Genet; 1996 Jun; 63(4):554-7. PubMed ID: 8826434 [TBL] [Abstract][Full Text] [Related]
56. [Epilepsy and psychomotor retardation in a child with aplasia cutis and brachydactyly (Adams-Oliver syndrome)]. Verdú Pérez A; Pantoja Bajo A; Alonso García LA; Garde Morales T An Esp Pediatr; 1996 Mar; 44(3):289-91. PubMed ID: 8830611 [No Abstract] [Full Text] [Related]
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58. Familial broad terminal phalanges with one individual showing additional anomalies. Pavone L; Sorge G; Pavone V; Rizzo R; Ruggieri M; Polizzi A; Opitz JM Am J Med Genet; 1997 Aug; 71(3):271-4. PubMed ID: 9268094 [TBL] [Abstract][Full Text] [Related]
59. Mandibulo-facial dysostosis with syndactyly. Mohanta KD; Panda TN Indian J Pediatr; 1970 Jun; 37(269):261-2. PubMed ID: 4319056 [No Abstract] [Full Text] [Related]