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TÃTULO: Dermatoscopic and clinical features of congenital or congenital-type nail matrix nevi: A multicenter prospective cohort study by the International Dermoscopy Society Full Text
AUTORES: Pham, Felix; Boespflug, Amelie; Duru, Gerard; Phan, Alice; Poulalhon, Nicolas; Weiler, Laura; Tanaka, Masaru; Lallas, Aimilios; Ogata, Dai; Davaine, Anne Celine; Bahadoran, Philippe; Balguerie, Xavier; Kaminska Winciorek, Grazyna; Tromme, Isabelle; Correia, Osvaldo; Kim, Moon Bum; Marghoob, Ashfaq A.; Martin, Linda; Guitera, Pascale; Meziane, Mariame; Miquel, Juliette; Mun, Je Ho; Argenziano, Giuseppe; Bessis, Didier; Bourke, Johnny; Mijuskovic, Zeljko; Chiaverini, Christine; Corven Benoit, Cloe; Droitcourt, Catherine; Skowron, Francois; Marque, Myriam; Zalaudek, Iris; Rosendahl, Cliff; Moreno Ramirez, David; Vabres, Pierre; Haenssle, Holger; Malvehy, Josep; Puig, Susana; Robert, Caroline; Schopf, Thomas R.; Scope, Alon; Dalle, Stephane; Thomas, Luc; ...Mais
PUBLICAÇÃO: 2022, FONTE: JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, VOLUME: 87, NÚMERO: 3

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TÃTULO: Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes Full Text
AUTORES: Sandy Leger; Xavier Balguerie; Alice Goldenberg; Valerie Drouin Garraud; Annick Cabot; Isabelle Amstutz Montadert; Paul Young; Pascal Joly; Virginie Bodereau; Muriel Holder Espinasse; Robyn V Jamieson; Amanda Krause; Hongsheng S Chen; Clarisse Baumann; Luis Nunes; Helene Dollfus; Michel Goossens; Veronique Pingault;
PUBLICAÇÃO: 2012, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 20, NÚMERO: 5

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WOS

TÃTULO: Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes Full Text
AUTORES: Sandy Léger; Xavier Balguerie; Alice Goldenberg; Valérie Drouin-Garraud; Annick Cabot; Isabelle Amstutz-Montadert; Paul Young; Pascal Joly; Virginie Bodereau; Muriel Holder-Espinasse; Robyn V Jamieson; Amanda Krause; Hongsheng Chen; Clarisse Baumann; Luis Nunes; Hélène Dollfus; Michel Goossens; Véronique Pingault;
PUBLICAÇÃO: 2012, FONTE: Eur J Hum Genet - European Journal of Human Genetics, VOLUME: 20, NÚMERO: 5

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