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13. Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature. Nazzaro A; Della Monica M; Lonardo F; Di Blasi A; Baffico M; Baldi M; Nazzaro G; De Placido G; Scarano G Prenat Diagn; 2004 Nov; 24(11):918-22. PubMed ID: 15565658 [TBL] [Abstract][Full Text] [Related]
14. Pfeiffer syndrome, type II. Herman TE; Siegel MJ J Perinatol; 2001 Dec; 21(8):565-7. PubMed ID: 11774022 [No Abstract] [Full Text] [Related]
15. Apert syndrome, an antenatal ultrasound detected case. Parent P; Le Guern H; Munck MR; Thoma M Genet Couns; 1994; 5(3):297-301. PubMed ID: 7811431 [TBL] [Abstract][Full Text] [Related]
17. A variant of Reinhardt-Pfeiffer mesomelic skeletal dysplasia. Bhatia M; Joseph B Pediatr Radiol; 2000 Mar; 30(3):184-5. PubMed ID: 10755759 [TBL] [Abstract][Full Text] [Related]
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19. Ultrasound detection of Apert syndrome: a case report and literature review. Kaufmann K; Baldinger S; Pratt L Am J Perinatol; 1997 Aug; 14(7):427-30. PubMed ID: 9263565 [TBL] [Abstract][Full Text] [Related]
20. [Type V acrocephalosyndactylia (Pfeiffer's syndrome). Apropos of 3 cases in the same family]. Manouvrier-Hanu S; Herbaux B; Pellerin P; Douchet P; Bouchez-Bonniere MC; Dubos JP; Farriaux JP Arch Fr Pediatr; 1989; 46(6):433-7. PubMed ID: 2783004 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]