kw.\*:("Dysostosis")
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DIE SPONDYLOCOSTALE DYSOSTOSE. BERICHT UEBER 5 BEOBACHTUNGEN EINSCHLIESSLICH GESCHWISTER UND EINEN ATYPISCHEN FALL = LA DYSOSTOSE SPONDYLOCOSTALE. 5 OBSERVATIONS, COMPRENANT DES FRERES ET SOEURS ET UN CAS ATYPIQUEPFEIFFER RA; HANSEN HG; BOEWING B et al.1983; MONATSSCHRIFT FUER KINDERHEILKUNDE; ISSN 0026-9298; DEU; DA. 1983; VOL. 131; NO 1; PP. 28-34; ABS. ENG; BIBL. 43 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
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
Acrofacial Dysostosis Syndrome Type Rodriguez : Prenatal Diagnosis and Autopsy FindingsSERMER, David; QUERCIA, Nada; CHONG, Karen et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 24, pp 3286-3289, issn 1552-4825, 4 p.Article
Newly recognized autosomal recessive acrofacial dysostosis syndrome resembling Nager syndromeKENNEDY, Shelley J; TEEBI, Ahmad S.American journal of medical genetics. 2004, Vol 129A, Num 1, pp 73-76, issn 0148-7299, 4 p.Article
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
Spondylocostal dysostosisYOUNG, I. D; MOORE, J. R.Journal of medical genetics. 1984, Vol 21, Num 1, pp 68-69, 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
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
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
Nager acrofacial dysostosis : An unusual association with both upper and lower eyelid colobomasTHAPA, Rajoo; PRAMANIK, Shanto; MUKHOPADHYAY, Maya et al.Indian journal of pediatrics. 2006, Vol 73, Num 7, pp 631-632, issn 0019-5456, 2 p.Article
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
Spatiotemporal disorder in the axial skeleton development of the Mesp2-null mouse: A model of spondylocostal dysostosis and spondylothoracic dysostosisMAKINO, Yuji; TAKAHASHI, Yu; SAGA, Yumiko et al.Bone (New York, NY). 2013, Vol 53, Num 1, pp 248-258, issn 8756-3282, 11 p.Article
Acrofacial dysostosis type rodríguezDIMITROV, Boyan; BALIKOVA, Irina; JEKOVA, Nely et al.American journal of medical genetics. 2005, Vol 135A, Num 1, pp 81-85, issn 0148-7299, 5 p.Article
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
LES SYNDROMES DE DYSOSTOSE SPONDYLO COSTALEBACHE MARIE BRIGITTE.1979; ; FRA; DA. 1979; 220; 56-(8) P.-PL.; 30 CM; BIBL. 42 REF.; TH.: MED./NANCY 1/1979Thesis
Laryngeal malformation in the Richieri-Costa-Pereira acrofacial dysostosis: Description of two new patientsTABITH, Alfredo JR; DE AZEVEDO BENTO-GONCALVES, Cristina Guedes.American journal of medical genetics. 2003, Vol 122A, Num 2, pp 133-138, issn 0148-7299, 6 p.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
Laryngeal Malformation in Richieri-Costa Pereira Syndrome: New FindingsCORACINE MIGUEL, Haline; GIACOMO CARNEIRO, Christiano; TABITH, Alfredo et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 8, pp 1967-1970, issn 1552-4825, 4 p.Article
Pseudodominant inheritance of spondylocostal dysostosis type 1 caused by two familial delta-like 3 mutationsWHITTOCK, N. V; ELLARD, S; DUNCAN, J et al.Clinical genetics. 2004, Vol 66, Num 1, pp 67-72, issn 0009-9163, 6 p.Article
DYSOSTOSE SPONDYLOCOSTALE AVEC POLYDACTYLIEZELLER C; BABIN E; DIETEMANN JL et al.1982; J. RADIOL.; ISSN 0242-3081; FRA; DA. 1982; VOL. 63; NO 5; PP. 355-357; ABS. ENG; BIBL. 9 REF.Article
CRANIOFACIAL SURGERY: PRESENT AND FUTURE.WHITAKER LA; RANDALL P; SCHUT L et al.1976; ANN. SURG.; U.S.A.; DA. 1976; VOL. 184; NO 5; PP. 558-564; BIBL. 15 REF.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
LA SYMPHALANGIE ET SA SIGNIFICATIONSEIGNEURIC C; SERRAD E; CORTET P et al.1982; ANN. RADIOL.; ISSN 0003-4185; FRA; DA. 1982; VOL. 25; NO 3; PP. 213-216; ABS. ENG; BIBL. 11 REF.Article