Browsing by Author Holder, Susan

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 1 of 1
Issue DateTitleAuthor(s)Citation
2014De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual DisabilityWilson, Meredith; Archer, Hayley; Canham, Natalie; Carss, Keren J; et al, Various; Firth, Helen; Grozeva, Detelina; Hackett, Anna; Holder, Susan; Park, Soo-Mi; Parker, Michael; Spasic-Boskovic, Olivera; Childrens Hospital Westmead: Paediatrics & Child HealthDe Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability, American Journal of Human Genetics, vol.94, 4, 2014,pp 618-624