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Robert S Wildin

Showing results (1-10 of 11) with videos related to

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The Journal of Applied Laboratory Medicine|January 3, 2024
Cost Effectiveness of Genomic Population Health Screening in Adults: A Review of Modeling Studies and Future DirectionsRobert S Wildin
Journal of Autoimmunity|October 26, 2005
IPEX and FOXP3: clinical and research perspectivesRobert S Wildin, Antonio Freitas
Journal of Community Genetics|October 4, 2023
Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screeningChristina A Hansen, Aaron W Reiter, Robert S Wildin
Pediatric Dermatology|December 16, 2020
Novel neonatal presentation of megalencephaly-polymicrogyria-pigmentary mosaicism syndrome (MPPM) related to MTOR mutation: Report of a caseDustin L Taylor, Robert S Wildin, Keith W Morley
Journal of Community Genetics|May 24, 2021
Modernizing family health history: achievable strategies to reduce implementation gapsRobert S Wildin, Donna J Messersmith, Elisa J F Houwink
Journal of Personalized Medicine|December 23, 2022
Real-World Results from Combined Screening for Monogenic Genomic Health Risks and Reproductive Risks in 300 AdultsRobert S Wildin, Diana L Gerrard, Debra G B Leonard
Frontiers in Genetics|May 13, 2022
Primary Care Implementation of Genomic Population Health Screening Using a Large Gene Sequencing PanelRobert S Wildin, Christine A Giummo, Aaron W Reiter, et al.
American Journal of Medical Genetics. Part A|September 24, 2005
Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long armLuke J Boyd, Joseph S Livingston, Michael G Brown, et al.
JCI Insight|October 5, 2016
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysisHani Bagheri, Chansonette Badduke, Ying Qiao, et al.
Blood|December 8, 2011
Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculatureJan Kazenwadel, Genevieve A Secker, Yajuan J Liu, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The Journal of Applied Laboratory Medicine|January 3, 2024
Cost Effectiveness of Genomic Population Health Screening in Adults: A Review of Modeling Studies and Future DirectionsRobert S Wildin
Journal of Autoimmunity|October 26, 2005
IPEX and FOXP3: clinical and research perspectivesRobert S Wildin, Antonio Freitas
Journal of Community Genetics|October 4, 2023
Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screeningChristina A Hansen, Aaron W Reiter, Robert S Wildin
Pediatric Dermatology|December 16, 2020
Novel neonatal presentation of megalencephaly-polymicrogyria-pigmentary mosaicism syndrome (MPPM) related to MTOR mutation: Report of a caseDustin L Taylor, Robert S Wildin, Keith W Morley
Journal of Community Genetics|May 24, 2021
Modernizing family health history: achievable strategies to reduce implementation gapsRobert S Wildin, Donna J Messersmith, Elisa J F Houwink
Journal of Personalized Medicine|December 23, 2022
Real-World Results from Combined Screening for Monogenic Genomic Health Risks and Reproductive Risks in 300 AdultsRobert S Wildin, Diana L Gerrard, Debra G B Leonard
Frontiers in Genetics|May 13, 2022
Primary Care Implementation of Genomic Population Health Screening Using a Large Gene Sequencing PanelRobert S Wildin, Christine A Giummo, Aaron W Reiter, et al.
American Journal of Medical Genetics. Part A|September 24, 2005
Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long armLuke J Boyd, Joseph S Livingston, Michael G Brown, et al.
JCI Insight|October 5, 2016
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysisHani Bagheri, Chansonette Badduke, Ying Qiao, et al.
Blood|December 8, 2011
Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculatureJan Kazenwadel, Genevieve A Secker, Yajuan J Liu, et al.
Pageof 2