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G Biesecker

Showing results (461-470 of 475) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2018
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite studyM Ragan Hart, Barbara B Biesecker, Carrie L Blout, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 24, 2019
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite studyM Ragan Hart, Barbara B Biesecker, Carrie L Blout, et al.
Genome Medicine|December 26, 2018
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controlsJung Kim, Wen Luo, Mingyi Wang, et al.
Transplantation|July 31, 2025
Further Personalizing Medicine in Immune Disorders: Genomic Findings and Hematopoietic Cell Transplantation SurvivalMorgan N Similuk, Sarah A Bannon, Jia Yan, et al.
American Journal of Human Genetics|March 2, 2005
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutationsJennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, et al.
American Journal of Human Genetics|September 3, 2021
Response to Hamosh et alLeslie G Biesecker, Margaret P Adam, Fowzan S Alkuraya, et al.
Medrxiv : the Preprint Server for Health Sciences|July 20, 2021
Genetic regulation of <i>OAS1</i> nonsense-mediated decay underlies association with risk of severe COVID-19A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
Human Mutation|July 31, 2010
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutationsJennifer J Johnston, Julie C Sapp, Joyce T Turner, et al.
American Journal of Human Genetics|January 8, 2021
A dyadic approach to the delineation of diagnostic entities in clinical genomicsLeslie G Biesecker, Margaret P Adam, Fowzan S Alkuraya, et al.
American Journal of Human Genetics|July 9, 2016
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic MedicineRobert C Green, Katrina A B Goddard, Gail P Jarvik, et al.
Pageof 48

Showing results (461-470 of 475) with videos related to

Sort By:
Pageof 48
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2018
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite studyM Ragan Hart, Barbara B Biesecker, Carrie L Blout, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 24, 2019
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite studyM Ragan Hart, Barbara B Biesecker, Carrie L Blout, et al.
Genome Medicine|December 26, 2018
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controlsJung Kim, Wen Luo, Mingyi Wang, et al.
Transplantation|July 31, 2025
Further Personalizing Medicine in Immune Disorders: Genomic Findings and Hematopoietic Cell Transplantation SurvivalMorgan N Similuk, Sarah A Bannon, Jia Yan, et al.
American Journal of Human Genetics|March 2, 2005
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutationsJennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, et al.
American Journal of Human Genetics|September 3, 2021
Response to Hamosh et alLeslie G Biesecker, Margaret P Adam, Fowzan S Alkuraya, et al.
Medrxiv : the Preprint Server for Health Sciences|July 20, 2021
Genetic regulation of <i>OAS1</i> nonsense-mediated decay underlies association with risk of severe COVID-19A Rouf Banday, Megan L Stanifer, Oscar Florez-Vargas, et al.
Human Mutation|July 31, 2010
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutationsJennifer J Johnston, Julie C Sapp, Joyce T Turner, et al.
American Journal of Human Genetics|January 8, 2021
A dyadic approach to the delineation of diagnostic entities in clinical genomicsLeslie G Biesecker, Margaret P Adam, Fowzan S Alkuraya, et al.
American Journal of Human Genetics|July 9, 2016
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic MedicineRobert C Green, Katrina A B Goddard, Gail P Jarvik, et al.
Pageof 48