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Journal of Community Genetics
|
June 20, 2020
Home testing for COVID-19: lessons from direct to consumer genetics
Theodore E Wilson, Colin Halverson
JIMD Reports
|
May 12, 2021
Consideration of a metabolic disorder in the differential of mild developmental delay: A case of nonketotic hyperglycinemia revisited 36 years later
Timothy F Tramontana, Theodore E Wilson, Bryan E Hainline
International Journal of Pediatric Otorhinolaryngology
|
January 17, 2020
Case report of two children with auditory neuropathy spectrum disorder related to a neurofascin (NFASC) gene variant
Jonathan L Harper, Theodore E Wilson, Ryan M Mitchell
Clinical Genetics
|
February 12, 2024
Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder
Khurram Liaqat, Kayla Treat, Theodore E Wilson, et al.
Pediatric Dermatology
|
October 22, 2019
Bathing suit ichthyosis: Two Burmese siblings and a review of the literature
Wendy Li, Kate E Oberlin, Theodore E Wilson, et al.
Child Neurology Open
|
August 2, 2023
A 2-Year-Old Child with Alazami Syndrome with Newly Reported Findings of Immune Deficiency, Periventricular Nodular Heterotopia, and Stroke; Broadening the Phenotype of Alazami
Kristin D Fauntleroy-Love, Theodore E Wilson, Nurcicek Padem, et al.
Journal of Genetic Counseling
|
October 3, 2022
An investigation of preceptors' perceptions of behavioral elements of "professionalism" among genetic counseling students
Paula Delk, Isabella Bowling, Courtney Schroeder, et al.
Journal of Genetic Counseling
|
March 16, 2021
Exploring parents' perceptions of the value of pediatric genetic counseling patient letters: A qualitative study presenting lessons learned
Courtney Brown, Katharine J Head, Jane Hartsock, et al.
European Journal of Medical Genetics
|
October 27, 2019
An adult female with 5q34-q35.2 deletion: A rare syndromic presentation of left ventricular non-compaction and congenital heart disease
Priyanka Arya, Theodore E Wilson, John J Parent, et al.
Molecular Genetics and Metabolism
|
August 11, 2023
Dicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders
Michael F Wangler, Barbara Lesko, Rejwi Dahal, et al.
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Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Journal of Community Genetics
|
June 20, 2020
Home testing for COVID-19: lessons from direct to consumer genetics
Theodore E Wilson, Colin Halverson
JIMD Reports
|
May 12, 2021
Consideration of a metabolic disorder in the differential of mild developmental delay: A case of nonketotic hyperglycinemia revisited 36 years later
Timothy F Tramontana, Theodore E Wilson, Bryan E Hainline
International Journal of Pediatric Otorhinolaryngology
|
January 17, 2020
Case report of two children with auditory neuropathy spectrum disorder related to a neurofascin (NFASC) gene variant
Jonathan L Harper, Theodore E Wilson, Ryan M Mitchell
Clinical Genetics
|
February 12, 2024
Further evidence of involvement of ITSN1 in autosomal dominant neurodevelopmental disorder
Khurram Liaqat, Kayla Treat, Theodore E Wilson, et al.
Pediatric Dermatology
|
October 22, 2019
Bathing suit ichthyosis: Two Burmese siblings and a review of the literature
Wendy Li, Kate E Oberlin, Theodore E Wilson, et al.
Child Neurology Open
|
August 2, 2023
A 2-Year-Old Child with Alazami Syndrome with Newly Reported Findings of Immune Deficiency, Periventricular Nodular Heterotopia, and Stroke; Broadening the Phenotype of Alazami
Kristin D Fauntleroy-Love, Theodore E Wilson, Nurcicek Padem, et al.
Journal of Genetic Counseling
|
October 3, 2022
An investigation of preceptors' perceptions of behavioral elements of "professionalism" among genetic counseling students
Paula Delk, Isabella Bowling, Courtney Schroeder, et al.
Journal of Genetic Counseling
|
March 16, 2021
Exploring parents' perceptions of the value of pediatric genetic counseling patient letters: A qualitative study presenting lessons learned
Courtney Brown, Katharine J Head, Jane Hartsock, et al.
European Journal of Medical Genetics
|
October 27, 2019
An adult female with 5q34-q35.2 deletion: A rare syndromic presentation of left ventricular non-compaction and congenital heart disease
Priyanka Arya, Theodore E Wilson, John J Parent, et al.
Molecular Genetics and Metabolism
|
August 11, 2023
Dicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders
Michael F Wangler, Barbara Lesko, Rejwi Dahal, et al.
Page
of 2