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Susan M White

Showing results (41-50 of 160) with videos related to

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Familial Cancer|February 27, 2007
An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutationAngela Arnold, Stewart Payne, Samantha Fisher, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
Maternal inheritance of BDNF deletion, with phenotype of obesity and developmental delay in mother and childBrooke E Harcourt, Denise V R Bullen, Kung-Ting Kao, et al.
Familial Cancer|May 9, 2018
Report of a bi-allelic truncating germline mutation in TP53Natasha J Brown, Kanika Bhatia, Julie Teague, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2022
Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and childrenIlias Goranitis, You Wu, Sebastian Lunke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectivenessZornitza Stark, Deborah Schofield, Melissa Martyn, et al.
Epilepsy Research|August 15, 2018
Corrigendum to "Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome" [Epilepsy Res. 140 (2018) 166-170]Kenneth A Myers, Susan M White, Shehla Mohammed, et al.
Epilepsy Research|January 26, 2018
Childhood-onset generalized epilepsy in Bainbridge-Ropers syndromeKenneth A Myers, Susan M White, Shehla Mohammed, et al.
American Journal of Medical Genetics. Part A|September 5, 2022
Elements of morphology: Standard terminology for the trunk and limbsLeslie G Biesecker, Margaret P Adam, Brian Hon-Yin Chung, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated familiesRavi Savarirayan, Susan M White, Frances R Goodman, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
The phenotype of Floating-Harbor syndrome in 10 patientsSusan M White, Angela Morgan, Annette Da Costa, et al.
Pageof 16

Showing results (41-50 of 160) with videos related to

Sort By:
Pageof 16
Familial Cancer|February 27, 2007
An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutationAngela Arnold, Stewart Payne, Samantha Fisher, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
Maternal inheritance of BDNF deletion, with phenotype of obesity and developmental delay in mother and childBrooke E Harcourt, Denise V R Bullen, Kung-Ting Kao, et al.
Familial Cancer|May 9, 2018
Report of a bi-allelic truncating germline mutation in TP53Natasha J Brown, Kanika Bhatia, Julie Teague, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2022
Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and childrenIlias Goranitis, You Wu, Sebastian Lunke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectivenessZornitza Stark, Deborah Schofield, Melissa Martyn, et al.
Epilepsy Research|August 15, 2018
Corrigendum to "Childhood-onset generalized epilepsy in Bainbridge-Ropers syndrome" [Epilepsy Res. 140 (2018) 166-170]Kenneth A Myers, Susan M White, Shehla Mohammed, et al.
Epilepsy Research|January 26, 2018
Childhood-onset generalized epilepsy in Bainbridge-Ropers syndromeKenneth A Myers, Susan M White, Shehla Mohammed, et al.
American Journal of Medical Genetics. Part A|September 5, 2022
Elements of morphology: Standard terminology for the trunk and limbsLeslie G Biesecker, Margaret P Adam, Brian Hon-Yin Chung, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated familiesRavi Savarirayan, Susan M White, Frances R Goodman, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
The phenotype of Floating-Harbor syndrome in 10 patientsSusan M White, Angela Morgan, Annette Da Costa, et al.
Pageof 16