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TÃTULO: Damaging de novo missense variants inEEF1A2lead to a developmental and degenerative epileptic-dyskinetic encephalopathy Full Text
AUTORES: Gemma L Carvill; Katherine L Helbig; Candace T Myers; Marcello Scala; Robert Huether; Sara Lewis; Tyler N Kruer; Brandon S Guida; Somayeh Bakhtiari; Joy Sebe; Sha Tang; Heather Stickney; Sehribani Ulusoy Oktay; Ashwin A Bhandiwad; Keri Ramsey; Vinodh Narayanan; Timothy Feyma; Luis O Rohena; Andrea Accogli; Mariasavina Severino; Georgina Hollingsworth; Deepak Gill; Christel Depienne; Caroline Nava; Lynette G Sadleir; Paul A Caruso; Angela E Lin ; Floor E Jansen; Bobby Koeleman; Eva Brilstra; Marjolein H Willemsen; Tjitske Kleefstra; Joaquim Sa; Marie Laure Mathieu; Laurine Perrin; Gaetan Lesca; Pasquale Striano; Giorgio Casari; Ingrid E Scheffer; David Raible; Evelyn Sattlegger; Valeria Capra; Sergio Padilla Lopez; Heather C Mefford; Michael C Kruer; ...Mais
PUBLICAÇÃO: 2020, FONTE: HUMAN MUTATION, VOLUME: 41, NÚMERO: 7

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TÃTULO: Further clinical and molecular delineation of the 15q24 microdeletion syndrome
AUTORES: Heather C Mefford; Jill A Rosenfeld; Natasha Shur; Anne M Slavotinek; Victoria A Cox; Raoul C Hennekam; Helen V Firth; Lionel Willatt; Patricia Wheeler; Eric M Morrow; Joseph Cook; Rachel Sullivan; Albert Oh; Marie T McDonald; Jonathan Zonana; Kory Keller; Mark C Hannibal; Susie Ball; Jennifer Kussmann; Jerome Gorski; Susan Zelewski; Valerie Banks; Wendy Smith; Rosemarie Smith; Lindsay Paull; Kenneth N Rosenbaum; David J Amor; Joao Silva; Allen Lamb; Evan E Eichler; ...Mais
PUBLICAÇÃO: 2012, FONTE: JOURNAL OF MEDICAL GENETICS, VOLUME: 49, NÚMERO: 2

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