Génétique et gène SHOX = SHOX gene and short-stature syndromesHUBER, C; CORMIER-DAIRE, V.Archives de pédiatrie (Paris). 2004, Vol 11, Num 6, pp 555-556, issn 0929-693X, 2 p.Conference Paper

Approche clinique de l'enfant dysmorphique = Clinical approach in dysmorphic childrenCORMIER-DAIRE, V.Archives de pédiatrie (Paris). 2001, Vol 8, pp 382s-384s, issn 0929-693X, SUP2Conference Paper

New insights in congenital bowing of the femoraCORMIER-DAIRE, V; GENEVIEVE, D; MUNNICH, A et al.Clinical genetics. 2004, Vol 66, Num 3, pp 169-176, issn 0009-9163, 8 p.Article

Schmid type metaphyseal chondrodysplasia : a spondylometaphyseal dysplasia identical to the Japanese typeSAVARIRAYAN, R; CORMIER-DAIRE, V; LACHMAN, R. S et al.Pediatric radiology. 2000, Vol 30, Num 7, pp 460-463, issn 0301-0449Article

Maladies osseuses constitutionnelles : Trente and de progrès en orthopédie pédiatrique = Thirty years of progress in pediatric orthopedicsFINIDORI, G; LE MERRER, M; CORMIER-DAIRE, V et al.Revue de chirurgie orthopédique et réparatrice de l'appareil moteur. 2006, Vol 92, Num 4, pp 382-383, issn 0035-1040, 2 p.Article

Revisiting Metatropic Dysplasia : Presentation of a Series of 19 Novel Patients and Review of the LiteratureGENEVIEVE, D; LE MERRER, M; FEINGOLD, J et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 8, pp 992-996, issn 1552-4825, 5 p.Article

Long-term follow-up in a patient with metatropic dysplasia. Author's replyGENEVIEVE, D; LE MERRER, M; MUNNICH, A et al.American journal of medical genetics. 2005, Vol 135A, Num 3, pp 342-343, issn 0148-7299, 2 p.Article

Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletionBAUD, O; CORMIER-DAIRE, V; LYONNET, S et al.Clinical genetics. 1999, Vol 55, Num 6, pp 478-482, issn 0009-9163Article

Spondylo-epi-metaphyseal dysplasia (SEMD) matrilin 3 type: homozygote matrilin 3 mutation in a novel form of SEMDBOROCHOWITZ, Z. U; SCHEFFER, D; ADIR, V et al.Journal of medical genetics. 2004, Vol 41, Num 5, pp 366-372, issn 0022-2593, 7 p.Article

Circonstances cliniques du diagnostic du syndrome de Smith-Lemli-Opitz et tentatives de corrélation phénotype-génotype: à propos de 45 cas = When should Smith-Lemli-Opitz syndrome be considered? A serie of 45 casesGOLDENBERG, A; CHEVY, F; BERNARD, C et al.Archives de pédiatrie (Paris). 2003, Vol 10, Num 1, pp 4-10, issn 0929-693X, 7 p.Article

Epiphyseal, vertebral, and ear (EVE) dysplasia : a new syndrome?AMIEL, J; CORMIER-DAIRE, V; JOURNEAU, P et al.Journal of medical genetics. 1999, Vol 36, Num 7, pp 561-564, issn 0022-2593Article

Acral dysostosis dyserythropoiesis syndromeLE MERRER, M; GIROT, R; PARENT, P et al.European journal of pediatrics. 1995, Vol 154, Num 5, pp 384-388, issn 0340-6199Article

Ostéogenèse imparfaite, annonce du diagnostic (classification clinique et génétique) = Osteogenesis imperfecta, diagnosis information (clinical and genetic classification)BAUJAT, G; LEBRE, A.-S; CORMIER-DAIRE, V et al.Archives de pédiatrie (Paris). 2008, Vol 15, Num 5, pp 789-791, issn 0929-693X, 3 p.Conference Paper

Le carbohydrate-deficient glycoprotein syndrome de type I : un nouvel éclairage sur le métabolisme du mannose = Mannose metabolism and carbohydrate deficient glycoprotein syndrome type ISETA, N; DUPRE, T; CORMIER-DAIRE, V et al.MS. Médecine sciences. 1999, Vol 15, Num 11, pp 1202-1210, issn 0767-0974Article

Prezygotic origin of the isochromosome 12p in Pallister-Killian syndromeCORMIER-DAIRE, V; LE MERRER, M; GIGAREL, N et al.American journal of medical genetics. 1997, Vol 69, Num 2, pp 166-168, issn 0148-7299Article

Non radioactive single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTP gene using the pharmacia phastsystemCORMIER-DAIRE, V; CLAVEL, C; POLETTE, M et al.Pathologie et biologie. 1993, Vol 41, Num 8, pp 713-715, issn 0369-8114Conference Paper

Sulphate transporter gene mutations in apparently isolated club footHUBER, C; ODENT, S; RUMEUR, S et al.Journal of medical genetics. 2001, Vol 38, Num 3, pp 191-192, issn 0022-2593Article

Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux typeFAIVRE, L; LE MERRER, M; MEGARBANE, A et al.Journal of medical genetics. 2000, Vol 37, Num 1, pp 52-54, issn 0022-2593Article

Genitopatellar syndrome : a new condition comprising absent patellae, scrotal hypoplasia, renal anomalies, facial dysmorphism, and mental retardationCORMIER-DAIRE, V; CHAUVET, M.-L; LYONNET, S et al.Journal of medical genetics. 2000, Vol 37, Num 7, pp 520-524, issn 0022-2593Article

Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyHARPEY, J.-P; HERON, D; PRUDENT, M et al.Journal of inherited metabolic disease. 1998, Vol 21, Num 7, pp 748-752, issn 0141-8955Article

Microsatellite DNA markers detects 95% of chromosome 22q11 deletionsBONNET, D; CORMIER-DAIRE, V; KACHANER, J et al.American journal of medical genetics. 1997, Vol 68, Num 2, pp 182-184, issn 0148-7299Article

Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylationCORMIER-DAIRE, V; CHRETIEN, D; RUSTIN, P et al.The Journal of pediatrics. 1997, Vol 130, Num 5, pp 817-822, issn 0022-3476Article

Autosomal Dominant Spondylocarpotarsal Synostosis Syndrome : Phenotypic Homogeneity and Genetic HeterogeneityISIDOR, B; CORMIER-DAIRE, V; LE MERRER, M et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 12, pp 1593-1597, issn 1552-4825, 5 p.Article

New mesomelic dysplasia with absent fibulae and triangular tibiaeSAVARIRAYAN, R; CORMIER-DAIRE, V; CURRY, C. J et al.American journal of medical genetics. 2000, Vol 94, Num 1, pp 59-63, issn 0148-7299Article

Craniosynostosis and kidney malformation in a case of Hennekan syndromeCORMIER-DAIRE, V; LYONNET, S; LEHNERT, A et al.American journal of medical genetics. 1995, Vol 57, Num 1, pp 66-68, issn 0148-7299Article