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Cyrus Boelman

Showing results (31-40 of 35) with videos related to

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Brain : a Journal of Neurology|August 23, 2015
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotypeFatima Jaffer, Andreja Avbersek, Rosaria Vavassori, et al.
HGG Advances|May 23, 2022
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES studyAlison M Elliott, Shelin Adam, Christèle du Souich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic testAnath C Lionel, Gregory Costain, Nasim Monfared, et al.
Genome Medicine|June 13, 2022
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndromeMargot A Cousin, Emma L Veale, Nikita R Dsouza, et al.
American Journal of Human Genetics|November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic EncephalopathiesFadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Brain : a Journal of Neurology|August 23, 2015
Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotypeFatima Jaffer, Andreja Avbersek, Rosaria Vavassori, et al.
HGG Advances|May 23, 2022
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES studyAlison M Elliott, Shelin Adam, Christèle du Souich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic testAnath C Lionel, Gregory Costain, Nasim Monfared, et al.
Genome Medicine|June 13, 2022
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndromeMargot A Cousin, Emma L Veale, Nikita R Dsouza, et al.
American Journal of Human Genetics|November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic EncephalopathiesFadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Pageof 4