Taila Hartley
AuthID: R-00F-EBZ
1
TITLE: De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures
AUTHORS: 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;
PUBLISHED: 2018, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 103, ISSUE: 1
AUTHORS: 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;
PUBLISHED: 2018, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 103, ISSUE: 1
INDEXED IN: 
WOS
WOS2
TITLE: Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada Full Text
AUTHORS: 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;
PUBLISHED: 2014, SOURCE: HEREDITARY CANCER IN CLINICAL PRACTICE, VOLUME: 12, ISSUE: 1
AUTHORS: 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;
PUBLISHED: 2014, SOURCE: HEREDITARY CANCER IN CLINICAL PRACTICE, VOLUME: 12, ISSUE: 1
