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G Biesecker

Showing results (201-210 of 475) with videos related to

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Cold Spring Harbor Molecular Case Studies|October 15, 2021
Case report: five-year experience of AKT inhibition with miransertib (MK-7075) in an individual with Proteus syndromeChristopher A Ours, Julie C Sapp, Mia B Hodges, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
Quantifying survival in patients with Proteus syndromeJulie C Sapp, Lian Hu, Jean Zhao, et al.
Journal of Nursing Scholarship : an Official Publication of Sigma Theta Tau International Honor Society of Nursing|January 9, 2013
Current and emerging technology approaches in genomicsYvette P Conley, Leslie G Biesecker, Stephen Gonsalves, et al.
Plos One|October 17, 2015
Characterization of Courtesy Stigma Perceived by Parents of Overweight Children with Bardet-Biedl SyndromeBarbara Hamlington, Lauren E Ivey, Ethan Brenna, et al.
Journal of Genetic Counseling|February 8, 2021
Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counselingLori H Erby, Tyler Wisniewski, Katie L Lewis, et al.
Clinical Genetics|December 25, 2004
Psychiatric and neuropsychological characterization of Pallister-Hall syndromeA Azzam, D M Lerner, K F Peters, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosisKim M Keppler-Noreuil, Eva H Baker, Julie C Sapp, et al.
American Journal of Medical Genetics|September 25, 1995
Detection of a subtle rearrangement of chromosome 22 using molecular techniquesL G Biesecker, M Rosenberg, L Dziadzio, et al.
Scientific Reports|December 15, 2015
Repression of AKT signaling by ARQ 092 in cells and tissues from patients with Proteus syndromeMarjorie J Lindhurst, Miranda R Yourick, Yi Yu, et al.
Human Molecular Genetics|August 22, 2023
Genome-wide identification of dominant polyadenylation hexamers for use in variant classificationHenoke K Shiferaw, Celine S Hong, David N Cooper, et al.
Pageof 48

Showing results (201-210 of 475) with videos related to

Sort By:
Pageof 48
Cold Spring Harbor Molecular Case Studies|October 15, 2021
Case report: five-year experience of AKT inhibition with miransertib (MK-7075) in an individual with Proteus syndromeChristopher A Ours, Julie C Sapp, Mia B Hodges, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
Quantifying survival in patients with Proteus syndromeJulie C Sapp, Lian Hu, Jean Zhao, et al.
Journal of Nursing Scholarship : an Official Publication of Sigma Theta Tau International Honor Society of Nursing|January 9, 2013
Current and emerging technology approaches in genomicsYvette P Conley, Leslie G Biesecker, Stephen Gonsalves, et al.
Plos One|October 17, 2015
Characterization of Courtesy Stigma Perceived by Parents of Overweight Children with Bardet-Biedl SyndromeBarbara Hamlington, Lauren E Ivey, Ethan Brenna, et al.
Journal of Genetic Counseling|February 8, 2021
Adaptation of the working alliance inventory for the assessment of the therapeutic alliance in genetic counselingLori H Erby, Tyler Wisniewski, Katie L Lewis, et al.
Clinical Genetics|December 25, 2004
Psychiatric and neuropsychological characterization of Pallister-Hall syndromeA Azzam, D M Lerner, K F Peters, et al.
American Journal of Medical Genetics. Part A|August 24, 2016
Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosisKim M Keppler-Noreuil, Eva H Baker, Julie C Sapp, et al.
American Journal of Medical Genetics|September 25, 1995
Detection of a subtle rearrangement of chromosome 22 using molecular techniquesL G Biesecker, M Rosenberg, L Dziadzio, et al.
Scientific Reports|December 15, 2015
Repression of AKT signaling by ARQ 092 in cells and tissues from patients with Proteus syndromeMarjorie J Lindhurst, Miranda R Yourick, Yi Yu, et al.
Human Molecular Genetics|August 22, 2023
Genome-wide identification of dominant polyadenylation hexamers for use in variant classificationHenoke K Shiferaw, Celine S Hong, David N Cooper, et al.
Pageof 48