Syndrome oro-facio-digital de type I (syndrome de Papillon-Léage) observé chez un octogénaire = Type I oral-facial-digital syndrome (Papillon-Léage syndrome) in an eighty-two-year-old womanDONNET, A; BAKCHINE, S; CHAIN, F et al.La Semaine des hôpitaux de Paris. 1989, Vol 65, Num 14, pp 888-890, issn 0037-1777Article

The orofaciodigital (OFD) syndromesBARAITSER, M.Journal of medical genetics. 1986, Vol 23, Num 2, pp 116-119, issn 0022-2593Article

Dysplasies et dystrophies osseuses. Le point de vue de l'anatomopathologiste = Bone dysplasia and dystrophy with regard from the pathologistCHOMETTE, G; AURIOL, M.Revue de stomatologie et de chirurgie maxillo-faciale. 1987, Vol 88, Num 1, pp 15-19, issn 0035-1768Article

Nager syndrome versus anomaly and its nosology with the postaxial acrofacial dysostosis syndrome of Genée and WiedemannOPITZ, J. M.American journal of medical genetics. 1987, Vol 27, Num 4, pp 959-963, issn 0148-7299Article

Robin sequence and oligodactyly in mother and son ― probably a further example of the postaxial acrofacial dysostosis syndrome. ReplyMEINECKE, P; WIEDEMANN, H.-R; ROBINOW, M et al.American journal of medical genetics. 1987, Vol 27, Num 4, pp 953-957, issn 0148-7299Article

Brief clinical report: acrofacial dysostosis with postaxial limb deficiencyFRYNS, J. P; VAN DEN BERGHE, H.American journal of medical genetics. 1988, Vol 29, Num 1, pp 205-208, issn 0148-7299Article

Postaxial acrofacial dysostosis (Miller) syndrome : a new caseVIGNERON, J; STRICKER, M; VERT, P et al.Journal of medical genetics. 1991, Vol 28, Num 9, pp 636-638, issn 0022-2593Article

Les syndromes oro-facio-digitaux = Orodigitofacial syndromesMANOUVRIER-HANU, S; FRARIAUX, J. P.Médecine et hygiène. 1989, Vol 47, Num 1782, pp 482-486, issn 0025-6749, 3 p.Article

The Nager syndromeHECHT, J. T; IMMKEN, L. L; HARRIS, L. F et al.American journal of medical genetics. 1987, Vol 27, Num 4, pp 965-969, issn 0148-7299Article

Acrodysostosis and protrusio acetabuli: an associationMACNICOL, M. F; MAKRIS, D.Journal of bone and joint surgery. British volume. 1988, Vol 70, Num 1, pp 38-39, issn 0301-620XArticle

The operative treatment of isolated craniofacial dysostosis (plagiocephaly) : a comparison of the unilateral and bilateral techniquesBARTLETT, S. P; WHITAKER, L. A; MARCHAC, D et al.Plastic and reconstructive surgery (1963). 1990, Vol 85, Num 5, pp 677-683, issn 0032-1052, 7 p.Article

Dysmorphogenesis of the mandible, zygoma, and middle ear ossicles in hemifacial microsomia and mandibulofacial dysostosisKAY, E. D; KAY, C. N.American journal of medical genetics. 1989, Vol 32, Num 1, pp 27-31, issn 0148-7299, 5 p.Article

Mutated MESP2 causes spondylocostal dysostosis in humansWHITTOCK, Neil V; SPARROW, Duncan B; WOUTERS, Merridee A et al.American journal of human genetics. 2004, Vol 74, Num 6, pp 1249-1254, issn 0002-9297, 6 p.Article

Evaluation of a uniform operative technique to treat syndactylyKERET, D; GER, E.The Journal of hand surgery (St. Louis, Mo.). 1987, Vol 12A, Num 5, pp 727-729, issn 0363-5023, 1Article

L'ostéoonychodysplasie, à propos de 1 cas révélé par une insuffisance rénale = A case of nail patella syndrome revealed by renale failureBERGAOUI, N; BEN DHIA N; LADEB, M. F et al.Rhumatologie (Aix-les-Bains). 1989, Vol 41, Num 7, pp 217-220, issn 0249-7581Article

Crouzon's syndrome (cranio-facial dysostosis): a case reportRAMA RAO, S; SUDHIR, M; GOPINATH, S. P et al.Clinician (Panjim). 1985, Vol 49, Num 12, pp 400-404, issn 0009-9341Article

Cervical spine in the apert syndromeKREIBORG, S; BARR, M. JR; MICHAEL COHEN, M. JR et al.American journal of medical genetics. 1992, Vol 43, Num 4, pp 704-708, issn 0148-7299Article

Syndrome de Franceschetti - Syndrome de Goldenhar = Franceschetti syndrome . Goldenhar syndromeFRANCESCHETTI, N; DUFIER, J.-L.Bulletin des sociétés d'ophtalmologie de France. 1995, Vol 95, Num 5, pp 307-309, issn 0081-1270Article

Spondylothoracic and spondylocostal dysostosis: hereditary forms of spinal deformityROBERTS, A. P; CONNER, A. N; TOLMIE, J. L et al.Journal of bone and joint surgery. British volume. 1988, Vol 70, Num 1, pp 123-126, issn 0301-620XArticle

Kraniosynostose-Operationen im Kindesalter = Craniosynostosis in children : Surgical and anaesthetic implicationsBERG, K; GRUNDMANN, U; WILHELM, W et al.AINS. Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie. 1997, Vol 32, Num 3, pp 138-150, issn 0939-2661Article

Crouzon's disease. II: Case report ― face and forehead advancement in two stagesLOSKEN, H. W; MORRIS, W. M. M; UYS, P. B et al.SAMJ. South African medical journal. 1989, Vol 75, Num 7, pp 320-323, issn 0256-9574, 4 p., supplArticle

Three-dimensional spiral CT of craniofacial malformations in childrenBINAGHI, Stefano; GUDINCHET, Francois; RILLIET, Benedict et al.Pediatric radiology. 2000, Vol 30, Num 12, pp 856-860, issn 0301-0449Article

TCOF1 mutations excluded from a role in other first and second branchial arch-related disordersSPLENDORE, Alessandra; PASSOS-BUENO, Maria Rita; JABS, Ethylin Wang et al.American journal of medical genetics. 2002, Vol 111, Num 3, pp 324-327, issn 0148-7299Article

Über das Pippow-Syndrom = La dysostose cheirolombaire = Pippow's syndromeKRETZSCHMAR, R.Der Radiologe (Berlin. Print). 1988, Vol 28, Num 6, pp 289-293, issn 0033-832XArticle

Nonoperative treatment of camptodactylyHORI, M; NAKAMURA, R; INOUE, G et al.The Journal of hand surgery (St. Louis, Mo.). 1987, Vol 12, Num 6, pp 1061-1065, issn 0363-5023Article