La geophagie = GeophagiaPINSARD, D; ODENT, S.Concours médical (Paris). 1990, Vol 112, Num 24, pp 2222-2225, issn 0010-5309, 4 p.Article

A new syndrome with ptosis, coloboma and mental retardationLE MAREC, B; ODENT, S; URVOY, M et al.Genetic counseling. 1992, Vol 3, Num 2, pp 119-120, issn 1015-8146Article

Le diabete gestationnel = Gestational diabetesPINSARD, D; ODENT, S; SIEMEN, C et al.Concours médical (Paris). 1992, Vol 114, Num 22, pp 1936-1939, issn 0010-5309Article

Triphalangeal thumb and split foot in the same familyLE MAREC, B; ODENT, S; TREGUIER, C et al.Genetic counseling. 1990, Vol 1, Num 3-4, pp 251-258Article

Répercussions du diagnostic prénatal: enquête auprès de 133 femmes ayant eu une amniocentèse au QuébecODENT, S; LAFRAMBOISE, R; GAGNE, R et al.La Semaine des hôpitaux de Paris. 1987, Vol 63, Num 3, pp 103-108, issn 0037-1777Article

Somatostatine et métabolisme glucidique: une revue mise à jour = Somatostatin and carbohydrate metabolism, an updated reviewPINSARD, D; ODENT, S; EMY, P et al.Revue française d'endocrinologie clinique, nutrition et métabolisme. 1988, Vol 29, Num 4-5, pp 511-522, issn 0048-8062Article

Identification of 28 novel mutations in the Bardet―Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous diseaseMULLER, Jean; STOETZEL, C; MEGARBANE, A et al.Human genetics. 2010, Vol 127, Num 5, pp 583-593, issn 0340-6717, 11 p.Article

Pediatric outcome of children with the prenatal diagnosis of isolated septal agenesisDAMAJ, L; BRUNEAU, B; FERRY, M et al.Prenatal diagnosis. 2010, Vol 30, Num 12-13, pp 1143-1150, issn 0197-3851, 8 p.Article

Le retard mental syndromique = Syndromic mental retardationODENT, S; PASQUIER, L; DE LA ROCHEBROCHARD, C et al.Archives de pédiatrie (Paris). 2008, Vol 15, Num 5, pp 705-707, issn 0929-693X, 3 p.Conference Paper

Embryonic expression of the human MID1 gene and its mutations in Opitz syndromePINSON, L; AUGE, J; AMIEL, J et al.Journal of medical genetics. 2004, Vol 41, Num 5, pp 381-386, issn 0022-2593, 6 p.Article

Solitary median maxillary central incisor syndrome: Clinical case with a novel mutation of Sonic HedgehogGARAVELLI, Livia; ZANACCA, C; CASELLI, G et al.American journal of medical genetics. 2004, Vol 127A, Num 1, pp 93-95, issn 0148-7299, 3 p.Article

Expression of the Sonic hedgehog (SHH) gene during early human development and phenotypic expression of new mutations causing holoprosencephalyODENT, S; ATTIE-BITACH, T; VEKEMANS, M et al.Human molecular genetics (Print). 1999, Vol 8, Num 9, pp 1683-1689, issn 0964-6906Article

Le KID syndrome (Keratitis, Ichthyosis, Deafness). A propos de 3 cas = The KID syndrome (keratitis, ichthysosis, deafness). About 3 cases reportLE MAREC, B; URVOY, M; TOULEMONT, P.-J et al.Bulletin des sociétés d'ophtalmologie de France. 1995, Vol 95, Num 5, pp 337-341, issn 0081-1270, 3 p.Article

Maladie de Refsum = Refsum's diseaseLE MAREC, B; URVOY, M; TOULEMONT, J.-P et al.Bulletin des sociétés d'ophtalmologie de France. 1995, Vol 95, Num 5, pp 320-322, issn 0081-1270Article

Molecular analysis of 53 fragile X families with the probe StB12.3PUISSANT, H; MALINGE, M. C; LARGET-PIET, A et al.American journal of medical genetics. 1994, Vol 53, Num 4, pp 370-373, issn 0148-7299Article

Etude de la perfusion continue de faibles doses d'héparine dans la prévention des complications liées aux cathéters dans la période néonatale = Study of continuous infusion of low doses of heparin in the prevention of complications of catheters during the neonatalBETREMIEUX, P; ODENT, S; PRIGENT, J. Y et al.Revue de pédiatrie (Paris). 1988, Vol 24, Num 7, pp 311-315, issn 0035-1644Article

Syndrome oto-palato-digital de type 1 atteignant cinq générations, relations avec la forme de type II = Oto-palato-digital type I syndrome in five generations. Differential diagnosis with type IILE MAREC, B; ODENT, S; BRACQ, E et al.Annales de génétique (Paris). 1988, Vol 31, Num 3, pp 155-161, issn 0003-3995Article

Progressive Osseous Heteroplasia: A Model for the Imprinting Effects of GNAS Inactivating Mutations in HumansLEBRUN, M; RICHARD, N; TAIEB, A et al.The Journal of clinical endocrinology and metabolism. 2010, Vol 95, Num 6, pp 3028-3038, issn 0021-972X, 11 p.Article

Embryology of neural tube defects : information provided by associated malformationsCABARET, A. S; LOGET, P; LOEUILLET, L et al.Prenatal diagnosis. 2007, Vol 27, Num 8, pp 738-742, issn 0197-3851, 5 p.Article

Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndromeBADENS, C; LACOSTE, C; ODENT, S et al.Clinical genetics. 2006, Vol 70, Num 1, pp 57-62, issn 0009-9163, 6 p.Article

Spectrum of NSD1 mutations in Sotos and Weaver syndromesRIO, M; CLECH, L; RAOUL, O et al.Journal of medical genetics. 2003, Vol 40, Num 6, pp 436-440, issn 0022-2593, 5 p.Article

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutationMARSH, D. J; COULON, V; RICHARDSON, A.-L et al.Human molecular genetics (Print). 1998, Vol 7, Num 3, pp 507-515, issn 0964-6906Article

L'interruption spontanée des grossesses de foetus mâles atteints dans l'incontinentia pigmenti: (à propos d'une famille) = Miscarriage of male fetuses in familial incontinentia pigmentiODENT, S; LE MAREC, B; SMAHI, A et al.Journal de gynécologie obstétrique et biologie de la reproduction. 1997, Vol 26, Num 6, pp 633-636, issn 0368-2315Article

Diagnostic rapide de la méningite tuberculeuse par Polymerase chain reaction. Une observation chez un nourrisson = Rapid diagnosis of tuberculosis meningitis by PCR. A case reportODENT, S; MINET, J; LELIEVRE, R et al.Pédiatrie (Marseille). 1993, Vol 48, Num 3, pp 229-231, issn 0031-4021Article

Les enfants nés de mères alcooliques = Alcoholic mothers neonatesROUSSEY, M; ODENT, S; DABADIE, A et al.La Semaine des hôpitaux de Paris. 1989, Vol 65, Num 20, pp 1274-1281, issn 0037-1777Article