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Research in Developmental Disabilities
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December 3, 2014
Activity and participation in children with neurofibromatosis type 1
Barbara A Johnson, Xiaoming Sheng, Amber S Perry, et al.
International Journal of Dermatology
|
July 22, 2014
Goltz syndrome and PORCN mosaicism
David A Stevenson, Meghan Chirpich, Yvonne Contreras, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
March 20, 2023
Single Versus Multigene Testing for Hereditary Hearing Loss: Use and Costs in a Commercially Insured Cohort
Peter K Moon, Z Jason Qian, David A Stevenson, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
August 6, 2013
Association of twinning and maternal age with major structural birth defects in Utah, 1999 to 2008
Renee A Rider, David A Stevenson, Janice E Rinsky, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2006
Familial congenital non-immune hydrops, chylothorax, and pulmonary lymphangiectasia
David A Stevenson, Theodore J Pysher, Robert M Ward, et al.
American Journal of Medical Genetics. Part A
|
January 27, 2010
Speech-language characteristics of children with neurofibromatosis type 1
Heather L Thompson, David H Viskochil, David A Stevenson, et al.
American Journal of Medical Genetics. Part A
|
November 29, 2023
Time to diagnosis in rapid exome/genome sequencing in the clinical inpatient setting
Alison Schildt, David A Stevenson, Linbo Yu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2017
Promoting appropriate genetic testing: the impact of a combined test review and consultative service
Carlos J Suarez, Linbo Yu, Natalie Downs, et al.
American Journal of Medical Genetics. Part A
|
June 24, 2004
Pseudoaminopterin syndrome and trisomy 9
David A Stevenson, Jasmine Low, Jerald King, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2025
Langerhans Cell Histiocytosis in Cardiofaciocutaneous Syndrome
Laura Keehan, Richard Sleightholm, Lianna J Marks, et al.
Page
of 17
Search research articles
Search
Showing results (21-30 of 166) with videos related to
Sort By:
Page
of 17
Research in Developmental Disabilities
|
December 3, 2014
Activity and participation in children with neurofibromatosis type 1
Barbara A Johnson, Xiaoming Sheng, Amber S Perry, et al.
International Journal of Dermatology
|
July 22, 2014
Goltz syndrome and PORCN mosaicism
David A Stevenson, Meghan Chirpich, Yvonne Contreras, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
March 20, 2023
Single Versus Multigene Testing for Hereditary Hearing Loss: Use and Costs in a Commercially Insured Cohort
Peter K Moon, Z Jason Qian, David A Stevenson, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
August 6, 2013
Association of twinning and maternal age with major structural birth defects in Utah, 1999 to 2008
Renee A Rider, David A Stevenson, Janice E Rinsky, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2006
Familial congenital non-immune hydrops, chylothorax, and pulmonary lymphangiectasia
David A Stevenson, Theodore J Pysher, Robert M Ward, et al.
American Journal of Medical Genetics. Part A
|
January 27, 2010
Speech-language characteristics of children with neurofibromatosis type 1
Heather L Thompson, David H Viskochil, David A Stevenson, et al.
American Journal of Medical Genetics. Part A
|
November 29, 2023
Time to diagnosis in rapid exome/genome sequencing in the clinical inpatient setting
Alison Schildt, David A Stevenson, Linbo Yu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2017
Promoting appropriate genetic testing: the impact of a combined test review and consultative service
Carlos J Suarez, Linbo Yu, Natalie Downs, et al.
American Journal of Medical Genetics. Part A
|
June 24, 2004
Pseudoaminopterin syndrome and trisomy 9
David A Stevenson, Jasmine Low, Jerald King, et al.
American Journal of Medical Genetics. Part A
|
November 1, 2025
Langerhans Cell Histiocytosis in Cardiofaciocutaneous Syndrome
Laura Keehan, Richard Sleightholm, Lianna J Marks, et al.
Page
of 17