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

SOME SKULL DEFORMITIES AND THEIR SRGICAL CORRECTION = DEFORMATIONS DU CRANE ET CORRECTION CHIRURGICALESMAIL JM.1974; BRIT. ORTHOPT. J.; G.B.; DA. 1974; VOL. 31; PP. 35-46; BIBL. 9REF.Article

METAPHYSEAL AND SPONDYLOMETAPHYSEAL CHONDRODYSPLASIASKOZLOWSKI K.1976; CLIN. ORTHOP. RELAT. RES.; U.S.A.; DA. 1976; VOL. 114; NO 1; PP. 83-93; BIBL. 25 REF.Article

Spondylo-costal dysplasia: a further report ― review of 14 casesKOZLOWSKI, K.RöFo. Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin. 1984, Vol 140, Num 2, pp 204-209, issn 0340-1618Article

Oro-facio-digital syndromes I and II: radiological methods for diagnosis and the clinical variationsANNEREN, G; ARVIDSON, B; GUSTAVSON, K.-H et al.Clinical genetics. 1984, Vol 26, Num 3, pp 178-186, issn 0009-9163Article

SPONDYLOCOSTAL DYSOSTOSIS IN SOUTH AFRICAN SISTERSBEIGHTON P; HORAN FT.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 1; PP. 23-25; BIBL. 8 REF.Article

ASPECTS RADIOLOGIQUES D'UNE DYSOSTOSE METAPHYSAIREBOUDOU A; COTONI P; PLEYBER JY et al.1973; J. RADIOL. ELECTROL. MED. NUCL.; FR.; DA. 1973; VOL. 54; NO 4; PP. 347Serial Issue

METAPHYSEAL DYSOSTOSIS. DESCRIPTION OF AN ULTRASTRUCTURAL DEFECT IN THE EPIPHYSEAL PLATE CHONDROCYTES. CASE REPORT = DYSOSTOSE METAPHYSAIRE: DESCRIPTION D'UNE ANOMALIE ULTRASTRUCTURALE DES CHONDROCYTES DU CARTILAGE EPIPHYSAIRECOOPER RR; PONSETI IV.1973; J. BONE JOINT SURG., AMER. ED.; U.S.A.; DA. 1973; VOL. 55; NO 3; PP. 485-495; BIBL. 17 REF.Serial Issue

METAPHYSEAL DYSOSTASIS, JANSEN TYPE = DYSOSTOSE METAPHYSAIRE DU TYPE JANSENARROYO SCOTOLIFF H.1973; J. BONE JOINT SURG., AMER. ED.; U.S.A.; DA. 1973; VOL. 55; NO 3; PP. 623-629; BIBL. 28REF.Serial Issue

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

Spondylocostal dysostosisYOUNG, I. D; MOORE, J. R.Journal of medical genetics. 1984, Vol 21, Num 1, pp 68-69, issn 0022-2593Article

Brief clinical report: anomalies in an infant with Nager acrofacial dysostosisKRAUSS, C. M; HASSELL, L. A; GANG, D. L et al.American journal of medical genetics. 1985, Vol 21, Num 4, pp 761-764, issn 0148-7299Article

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

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

Another new form, the Palagonia type of acrofacial dysostosis in a Sicilian familySORGE, G; PAVONE, L; POLIZZI, A et al.American journal of medical genetics. 1997, Vol 69, Num 4, pp 388-394, issn 0148-7299Article

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

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

Cranial base dynamics in craniofacial dysostosisROSEN, H. M; WHITAKER, L. A.Journal of maxillofacial surgery. 1984, Vol 12, Num 2, pp 56-61, issn 0301-0503Article

Acrofacial dysostoses : review and report of a previously undescribed condition : the autosomal or X-linked dominant catania form of acrofacial dysostosisOPITZ, J. M; MOLLICA, F; SORGE, G et al.American journal of medical genetics. 1993, Vol 47, Num 5, pp 660-678, issn 0148-7299Article

METAPHYSEAL DYSOSTOSIS. A ROUGH SURFACED ENDOPLASMIC RETICULUM STORAGE DEFECT = DYSOSTOSE METAPHYSAIRE. UNE THESAUROSE DU RETICULUM ENDOPLASMIQUE A SURFACE RUGUEUSECOOPER RR; PEDRINI MILLE A; PONSETI IV et al.1973; LAB. INVEST.; U.S.A.; DA. 1973; VOL. 28; NO 1; PP. 119-125; BIBL. 20 REF.Serial Issue

Confirmation of the catania brachydactylous type of acrofacial dysostosis : Report of a second familyWULFSBERG, E. A; CAMPBELL, A. B; LURIE, I. W et al.American journal of medical genetics. 1996, Vol 63, Num 4, pp 554-557, issn 0148-7299Article

Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patientsCHRZANOWSKA, K. H; FRYNS, J. P; KRAJEWSKA-WALASEK, M et al.Clinical genetics. 1989, Vol 35, Num 2, pp 157-160, issn 0009-9163Article

FAMILIAL MANDIBULOACRAL DYSPLASIAZINA AM; CRAVARIO A; BUNDINO S et al.1981; BR. J. DERMATOL. (1951); ISSN 0007-0963; GBR; DA. 1981; VOL. 105; NO 6; PP. 719-723; BIBL. 8 REF.Article

POSTAXIAL ACROFACIAL DYSOSTOSIS SYNDROMEMILLER M; FINEMAN R; SMITH DW et al.1979; J. PEDIATR.; USA; DA. 1979; VOL. 95; NO 6; PP. 970-975; BIBL. 10 REF.Article