Taila Hartley
AuthID: R-00F-EBZ
1
TÃTULO: De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures
AUTORES: Yoko Ito; Keren J Carss; Sofia T Duarte; Taila Hartley; Boris Keren; Manju A Kurian; Isabelle Marey; Perinne Charles; Carla Mendonca; Caroline Nava; Rolph Pfundt; Alba Sanchis Juan; Hans van Bokhoven; Anthony van Essen; Conny van Ravenswaaij Arts; Kym M Boycott; Kristin D Kernohan; Sarah Dyack; Lucy L Raymond;
PUBLICAÇÃO: 2018, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 103, NÚMERO: 1
AUTORES: Yoko Ito; Keren J Carss; Sofia T Duarte; Taila Hartley; Boris Keren; Manju A Kurian; Isabelle Marey; Perinne Charles; Carla Mendonca; Caroline Nava; Rolph Pfundt; Alba Sanchis Juan; Hans van Bokhoven; Anthony van Essen; Conny van Ravenswaaij Arts; Kym M Boycott; Kristin D Kernohan; Sarah Dyack; Lucy L Raymond;
PUBLICAÇÃO: 2018, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 103, NÚMERO: 1
INDEXADO EM: 
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TÃTULO: Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada Full Text
AUTORES: Taila Hartley; Luca Cavallone; Nelly Sabbaghian; Rachel Silva Smith; Nancy Hamel; Olga Aleynikova; Erika Smith; Valerie Hastings; Pedro Pinto; Marc Tischkowitz; Eva Tomiak; William D Foulkes;
PUBLICAÇÃO: 2014, FONTE: HEREDITARY CANCER IN CLINICAL PRACTICE, VOLUME: 12, NÚMERO: 1
AUTORES: Taila Hartley; Luca Cavallone; Nelly Sabbaghian; Rachel Silva Smith; Nancy Hamel; Olga Aleynikova; Erika Smith; Valerie Hastings; Pedro Pinto; Marc Tischkowitz; Eva Tomiak; William D Foulkes;
PUBLICAÇÃO: 2014, FONTE: HEREDITARY CANCER IN CLINICAL PRACTICE, VOLUME: 12, NÚMERO: 1
