Pfeiffer type cardiocranial syndrome and van nesselrooij syndrome : Variable manifestations of a single disorder?RASALAM, Adelene D; DEAN, John C. S.American journal of medical genetics. 2005, Vol 132A, Num 2, issn 0148-7299, p. 209Article

Pfeiffer Syndrome: A Treatment EvaluationFEARON, Jeffrey A; RHODES, Jennifer.Plastic and reconstructive surgery (1963). 2009, Vol 123, Num 5, pp 1560-1569, issn 0032-1052, 10 p.Article

Patient with Pfeiffer's syndrome treated by midfacial distraction and comprehensive orthodonticsPARK, Yongjong; HOBAR, Paul C; SINN, Douglas P et al.American journal of orthodontics and dentofacial orthopedics. 2011, Vol 139, Num 2, pp 260-270, issn 0889-5406, 11 p.Article

Spinal anomalies in Pfeiffer syndromeMOORE, M. H; LODGE, M. L; CLARK, B. E et al.The Cleft palate-craniofacial journal. 1995, Vol 32, Num 3, pp 251-254, issn 1055-6656Article

A C.1019A > G Mutation in FGFR2, Which Predicts p.Tyr340Cys, in a Lethally Malformed Fetus With Pfeiffer Syndrome and Multiple PterygiaBAYNAM, Gareth; SMITH, Nicholas; GOLDBLATT, Jack et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 17, pp 2301-2303, issn 1552-4825, 3 p.Article

Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosisCOHEN, M. M.American journal of medical genetics. 1993, Vol 45, Num 3, pp 300-307, issn 0148-7299Article

Prenatal diagnosis of Pfeiffer syndrome type IIBLAUMEISER, Bettina; LOQUET, Philip; WUYTS, Wim et al.Prenatal diagnosis. 2004, Vol 24, Num 8, pp 644-646, issn 0197-3851, 3 p.Article

Pfeiffer syndrome : a syndrome of acrocephalosyndactylyKISSEL, C. G; GODDMAN, E. F; BOFFELI, T. J et al.The Journal of foot surgery. 1992, Vol 31, Num 2, pp 149-153, issn 0449-2544Article

Prenatal diagnosis of cloverleaf skull: Watch the hands!GORINCOUR, Guillaume; RYPENS, Francoise; GRIGNON, Andrée et al.Fetal diagnosis and therapy. 2005, Vol 20, Num 4, pp 296-300, issn 1015-3837, 5 p.Article

FGFR2 exon IIIa and III c mutations in Crouzon, Jackson-Weiss, and pfeiffer syndromes : Evidence for missense changes, insertions, and a deletion due to alternative RNA splicingMEYERS, G. A; DAY, D; SCOTT, A. F et al.American journal of human genetics. 1996, Vol 58, Num 3, pp 491-498, issn 0002-9297Article

Pfeiffer type cardiocranial syndrome : a third case reportWILLIAMSON-KRUSE, L; BIESECKER, L. G.Journal of medical genetics. 1995, Vol 32, Num 11, pp 901-903, issn 0022-2593Article

Dermatoglifos en 8 casos de sindrome de Pfeiffer = Dermatoglyphes dans 8 cas de syndrome de Pfeiffer = Dermatoglyphes in 8 cases of Pfeiffer syndromeBORBOLLA VACHER, L; HERNANDEZ IGLESIAS, M.Revista cubana de pediatría. 1989, Vol 61, Num 1, pp 9-20, issn 0034-7531Article

Arnold-Chiari malformation in an infant with Kleeblattschadel: an acquired malformation?VENES, J. L.Neurosurgery. 1988, Vol 23, Num 3, pp 360-362, issn 0148-396XArticle

Mesomelic Dysplasia With Acral Synostoses Verloes―David―Pfeiffer Type: Follow-Up Study Documents Progressive Clinical CourseISIDOR, Bertrand; HAMEL, Antoine; PLASSCHAERT, Frank et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 10, pp 2220-2225, issn 1552-4825, 6 p.Article

Pfeiffer's syndrome family tree : review of the literatureLYON, J. R; BURGESS, R. C.Clinical orthopaedics and related research. 1993, Num 294, pp 294-298, issn 0009-921XArticle

Spontaneous mutation and parental age in humansRISCH, N; REICH, E. W; WISHNICK, M. M et al.American journal of human genetics. 1987, Vol 41, Num 2, pp 218-248, issn 0002-9297Article

Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndromeLAJEUNIE, Elisabeth; HEUERTZ, Solange; EL GHOUZZI, Vincent et al.European journal of human genetics. 2006, Vol 14, Num 3, pp 289-298, issn 1018-4813, 10 p.Article

A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 geneSHOTELERSUK, Vorasuk; SRIVUTHANA, Sumarlee; ITTIWUT, Chupong et al.Southeast Asian journal of tropical medicine and public health. 2001, Vol 32, Num 2, pp 425-428, issn 0125-1562Article

Monobloc distraction osteogenesis during infancy : Report of a case and presentation of a new deviceCOHEN, S. R; BOYDSTON, W; BURSTEIN, F. D et al.Plastic and reconstructive surgery (1963). 1998, Vol 101, Num 7, pp 1919-1924, issn 0032-1052Article

Maxillary distraction osteogenesis in Pfeiffer's syndrome : urgent ocular protection by gradual midfacial skeletal advancementBRITTO, J. A; EVANS, R. D; HAYWARD, R. D et al.British journal of plastic surgery. 1998, Vol 51, Num 5, pp 343-349, issn 0007-1226Article

Congenital tracheal cartilaginous sleeveLIN, S. Y; JIANN-CHYUAN CHEN; HOTALING, A. J et al.The Laryngoscope. 1995, Vol 105, Num 11, pp 1213-1219, issn 0023-852XArticle

Atypical iris colobomata and Pfeiffer syndromeJONES, M. R; DE SA, L. C. F; GOOD, W. V et al.Journal of pediatric ophthalmology and strabismus. 1993, Vol 30, Num 4, pp 266-267, issn 0191-3913Article

Antecedent manipulation in the treatment of primary solid food refusalJOHNSON, C. R; BABBITT, R. L.Behavior modification. 1993, Vol 17, Num 4, pp 510-521, issn 0145-4455Article

l'acrocéphalosyndactylie de type V (syndrome de Pfeiffer): à propos de 3 cas dans une même famille = Type V acrocephalosyndactyly. Three cases in a some familyMANOUVRIER-HANU, S; HERBAUX, B; PELLERIN, P et al.Archives françaises de pédiatrie. 1989, Vol 46, Num 6, pp 433-437, issn 0003-9764Article

Rubrique iconographique dirigée par C. Fauré et J. Ph. Montagne: syndrome de Pfeiffer = Pfeiffer syndrome: radiological case reportLANTERI, M; BONIOLI, E; RUFFA, G et al.Archives françaises de pédiatrie. 1985, Vol 42, Num 8, pp 717-718, issn 0003-9764Article