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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
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
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
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
UNE FORME PARTICULIERE DE DYSOSTOSE CRANIO-FACIO-MANDIBULAIRE AVEC BRACHYDACTYLIE TYPE BVAN DAMME W; TOUITOU D.1979; J. MED. STRASBOURG; FRA; DA. 1979; VOL. 10; NO 2; PP. 105-109; ABS. ENG; BIBL. 17 REF.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
Polydactyly of the footPHELPS, D. A; GROGAN, D. P.Journal of pediatric orthopedics. 1985, Vol 5, Num 4, pp 446-451, issn 0271-6798Article
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
Nager's acrofacial dysostosis with thumb duplication: report of a caseGIUGLIANI, R; HELLER PEREIRA, C.Clinical genetics. 1984, Vol 26, Num 3, pp 228-230, issn 0009-9163Article
EXPERIENCE TREATING SYNDACTYLYMICALI G.1982; ANN. PLAST. SURG.; ISSN 0148-7043; USA; DA. 1982; VOL. 9; NO 1; PP. 65-71; BIBL. 21 REF.Article
A PROPOS DE DEUX CAS DE DYSOSTOSE MANDIBULO-FACIALELASAUSSE BERNARD.sd; FRA; DA. S.D.; 223; 39-VI P.-PL.; 30 CM; BIBL. 81 REF.; TH.: MED./PARIS 6/1979Thesis
THE CONTINUITY OF MANDIBULAR FORM IN MANDIBULOFACIAL DYSOSTOSISBEHRENTS RG.1982; J. DENT. RES.; ISSN 0022-0345; USA; DA. 1982; VOL. 61; NO 11; PP. 1240-1242; BIBL. 10 REF.Article
ACROFACIAL DYSOSTOSIS (NAGER SYNDROME): SYNOPSIS AND REPORT OF A NEW CASEPFEIFFER RA; STOESS H.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 2; PP. 255-260; BIBL. 28 REF.Article
HEREDITARY ONCHYO-OSTEO-DYSPLASIA (HOOD SYNDROME): REPORT OF TWO CASESGARCES MA; MURASKAS JK; MURASKAS EK et al.1982; SKELET. RADIOL.; ISSN 0364-2348; DEU; DA. 1982; VOL. 8; NO 1; PP. 55-58; BIBL. 8 REF.Article
Novel complex disease allele mutations in cleidocranial dysplasia patientsANTHONAPPA, Robert P; YAN-HUI, Fan; KING, Nigel M et al.Journal of oral pathology & medicine. 2014, Vol 43, Num 10, pp 798-800, issn 0904-2512, 3 p.Article