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David T Miller

Showing results (81-90 of 107) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2021
Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Adam S Gordon, et al.
Carcinogenesis|October 27, 2025
Symposium report-ethical and social considerations regarding return of secondary findings in atomic bomb survivorsNoriaki Yoshida, Douglas R Stewart, Arikuni Uchimura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2012
Exploring concordance and discordance for return of incidental findings from clinical sequencingRobert C Green, Jonathan S Berg, Gerard T Berry, et al.
Nature Methods|May 28, 2025
SAVANA: reliable analysis of somatic structural variants and copy number aberrations using long-read sequencingHillary Elrick, Carolin M Sauer, Jose Espejo Valle-Inclan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 23, 2022
The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2Abbe Lai, Aubrie Soucy, Christelle Moufawad El Achkar, et al.
Circulation|July 13, 2016
Clinical Trial of the Protein Farnesylation Inhibitors Lonafarnib, Pravastatin, and Zoledronic Acid in Children With Hutchinson-Gilford Progeria SyndromeLeslie B Gordon, Monica E Kleinman, Joe Massaro, et al.
The New England Journal of Medicine|January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss, Yiping Shen, Joshua M Korn, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
Pageof 11

Showing results (81-90 of 107) with videos related to

Sort By:
Pageof 11
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2021
Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Adam S Gordon, et al.
Carcinogenesis|October 27, 2025
Symposium report-ethical and social considerations regarding return of secondary findings in atomic bomb survivorsNoriaki Yoshida, Douglas R Stewart, Arikuni Uchimura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2021
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)David T Miller, Kristy Lee, Wendy K Chung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2012
Exploring concordance and discordance for return of incidental findings from clinical sequencingRobert C Green, Jonathan S Berg, Gerard T Berry, et al.
Nature Methods|May 28, 2025
SAVANA: reliable analysis of somatic structural variants and copy number aberrations using long-read sequencingHillary Elrick, Carolin M Sauer, Jose Espejo Valle-Inclan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 23, 2022
The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2Abbe Lai, Aubrie Soucy, Christelle Moufawad El Achkar, et al.
Circulation|July 13, 2016
Clinical Trial of the Protein Farnesylation Inhibitors Lonafarnib, Pravastatin, and Zoledronic Acid in Children With Hutchinson-Gilford Progeria SyndromeLeslie B Gordon, Monica E Kleinman, Joe Massaro, et al.
The New England Journal of Medicine|January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss, Yiping Shen, Joshua M Korn, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
Pageof 11