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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 Directions
Robert S Wildin
Journal of Autoimmunity
|
October 26, 2005
IPEX and FOXP3: clinical and research perspectives
Robert 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 screening
Christina 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 case
Dustin L Taylor, Robert S Wildin, Keith W Morley
Journal of Community Genetics
|
May 24, 2021
Modernizing family health history: achievable strategies to reduce implementation gaps
Robert 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 Adults
Robert 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 Panel
Robert 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 arm
Luke 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 analysis
Hani 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 vasculature
Jan Kazenwadel, Genevieve A Secker, Yajuan J Liu, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 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 Directions
Robert S Wildin
Journal of Autoimmunity
|
October 26, 2005
IPEX and FOXP3: clinical and research perspectives
Robert 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 screening
Christina 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 case
Dustin L Taylor, Robert S Wildin, Keith W Morley
Journal of Community Genetics
|
May 24, 2021
Modernizing family health history: achievable strategies to reduce implementation gaps
Robert 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 Adults
Robert 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 Panel
Robert 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 arm
Luke 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 analysis
Hani 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 vasculature
Jan Kazenwadel, Genevieve A Secker, Yajuan J Liu, et al.
Page
of 2