Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing
Mouden, C., Dubourg, C., Carré, W., Rose, S., Quelin, C., Akloul, L., Hamdi-Rozé, H., Viot, G., Salhi, H., Darnault, P., Odent, S., Dupé, V., David, V.
Published in Clinical genetics (01.06.2016)
Published in Clinical genetics (01.06.2016)
Get full text
Journal Article
Fetal phenotypes in otopalatodigital spectrum disorders
Naudion, S., Moutton, S., Coupry, I., Sole, G., Deforges, J., Guerineau, E., Hubert, C., Deves, S., Pilliod, J., Rooryck, C., Abel, C., Le Breton, F., Collardeau-Frachon, S., Cordier, M.P., Delezoide, A.L., Goldenberg, A., Loget, P., Melki, J., Odent, S., Patrier, S., Verloes, A., Viot, G., Blesson, S., Bessières, B., Lacombe, D., Arveiler, B., Goizet, C., Fergelot, P.
Published in Clinical genetics (01.03.2016)
Published in Clinical genetics (01.03.2016)
Get full text
Journal Article
Adverse obstetric and perinatal outcome with in vitro fertilization technology: A French nationwide population-based study
Pessione, F, De Mouzon, J, Deveaux, A, Epelboin, S, Gervoise-Boyer, M-J, Jimenez, C, Levy, R, Valentin, M, Viot, G, Bergère, M, Merlet, F, Jonveaux, P
Published in Gynécologie, obstétrique, fertilité & sénologie (01.04.2020)
Published in Gynécologie, obstétrique, fertilité & sénologie (01.04.2020)
Get full text
Journal Article
Inverted duplication with deletion: First interstitial case suggesting a novel undescribed mechanism of formation
Milosevic, J., El Khattabi, L., Roubergue, A., Coussement, A., Doummar, D., Cuisset, L., Le Tessier, D., Flageul, B., Viot, G., Lebbar, A., Dupont, J.M.
Published in American journal of medical genetics. Part A (01.12.2014)
Published in American journal of medical genetics. Part A (01.12.2014)
Get full text
Journal Article
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases
Chassaing, N., Cluzeau, C., Bal, E., Guigue, P., Vincent, M-C., Viot, G., Ginisty, D., Munnich, A., Smahi, A., Calvas, P.
Published in British journal of dermatology (1951) (01.05.2010)
Published in British journal of dermatology (1951) (01.05.2010)
Get full text
Journal Article
Decreasing birth defect in children by using high magnification selected spermatozoon injection
Cassuto, N.G, Hazout, A, Benifla, J.L, Balet, R, Larue, L, Viot, G
Published in Fertility and sterility (01.09.2011)
Published in Fertility and sterility (01.09.2011)
Get full text
Journal Article
Atypical findings in Kabuki syndrome: Report of 8 patients in a series of 20 and review of the literature
Geneviève, D., Amiel, J., Viot, G., Le Merrer, M., Sanlaville, D., Urtizberea, A., Gérard, M., Munnich, A., Cormier‐Daire, V., Lyonnet, Stanislas
Published in American journal of medical genetics. Part A (15.08.2004)
Published in American journal of medical genetics. Part A (15.08.2004)
Get full text
Journal Article
Perinatal outcome of 2140 singletons born from transfer of frozen-thawed embryos (FET) conceived by assisted reproductive technology (ART): a French control study 1998-2008
Epelboin, S, Devouche, E, Pejoan, H, Viot, G, Apter-Danon, G
Published in Fertility and sterility (2010)
Published in Fertility and sterility (2010)
Get full text
Journal Article
Prenatal diagnosis of a cleft of the tongue, lower lip and mandible
Vincent‐Rohfritsch, A., Anselem, O., Grangé, G., Benard, C., Viot, G., Lalau, P., Millischer‐Bellaïche, A. E., Hornoy, P., Mitrofanoff, M., Tsatsaris, V.
Published in Ultrasound in obstetrics & gynecology (01.01.2012)
Published in Ultrasound in obstetrics & gynecology (01.01.2012)
Get full text
Journal Article
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies
ISERIN, L, DE LONLAY, P, VIOT, G, SIDI, D, KACHANER, J, MUNNICH, A, LYONNET, S, VEKEMANS, M, BONNET, D
Published in European journal of pediatrics (01.11.1998)
Published in European journal of pediatrics (01.11.1998)
Get full text
Journal Article
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia
Taillandier, A., Lia-Baldini, A.S., Mouchard, M., Robin, B., Muller, F., Simon-Bouy, B., Serre, J.L., Bera-Louville, A., Bonduelle, M., Eckhardt, J., Gaillard, D., Myhre, A.G., Körtge-Jung, S., Larget-Piet, L., Malou, E., Sillence, D., Temple, I.K., Viot, G., Mornet, E.
Published in Human mutation (01.07.2001)
Published in Human mutation (01.07.2001)
Get full text
Journal Article
Late onset microcephaly: failure of prenatal diagnosis
Le Ray, C., Viot, G., Tsatsaris, V., Adamsbaum, C., Grangé, G.
Published in Ultrasound in obstetrics & gynecology (01.09.2004)
Published in Ultrasound in obstetrics & gynecology (01.09.2004)
Get full text
Journal Article
Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygroma
Pannier, E., Viot, G., Aubry, M. C., Grange, G., Tantau, J., Fallet-Bianco, C., Muller, F., Cabrol, D.
Published in Prenatal diagnosis (01.01.2003)
Published in Prenatal diagnosis (01.01.2003)
Get full text
Journal Article
Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1
Thauvin-Robinet, C, El Ghouzzi, V, Chemaitilly, W, Dagoneau, N, Boute, O, Viot, G, Mégarbané, A, Sefiani, A, Munnich, A, Le Merrer, M, Cormier-Daire, V
Published in Journal of medical genetics (01.10.2002)
Published in Journal of medical genetics (01.10.2002)
Get full text
Journal Article
Prenatal diagnosis of fetal tail and postabortum anatomical description
Grangé, G., Tantau, J., Pannier, E., Aubry, M.‐C., Viot, G., Fallet‐Bianco, C., Terrasse, G., Cabrol, D.
Published in Ultrasound in obstetrics & gynecology (01.11.2001)
Published in Ultrasound in obstetrics & gynecology (01.11.2001)
Get full text
Journal Article
Approche moléculaire de la prise en charge des immobilismes fœtaux et hypotonie néonatale
Get full text
Journal Article
Conference Proceeding