Search research articles
Contact Us
Filters
Showing results (21-30 of 86) with videos related to
Page
of 9
Sort By:
American Journal of Medical Genetics. Part A
|
September 21, 2016
Importance of a specialty clinic for individuals with fragile X syndrome
Jeannie Visootsak, Sharon A Kidd, Tovi Anderson, et al.
Pediatric Pulmonology
|
December 5, 2009
Congenital central hypoventilation syndrome: neurocognitive functioning in school age children
Frank A Zelko, Michael N Nelson, Sue E Leurgans, et al.
American Journal on Intellectual and Developmental Disabilities
|
October 27, 2025
FMR1 Premutation Carrier Mothers' Daily Negative Affect and Cortisol: Probing the Impacts of Stress Exposure, Coping Style, and CGG Repeats
Leann Smith DaWalt, Jinkuk Hong, Catherine Rogers Gaspar, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis
Brion S Maher, Mary L Marazita, Casey Rand, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 9, 2010
An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management
Debra E Weese-Mayer, Elizabeth M Berry-Kravis, Isabella Ceccherini, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
November 6, 2010
Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers
Lawrence J Jennings, Min Yu, Lili Zhou, et al.
American Journal of Medical Genetics. Part A
|
February 21, 2008
Genetic variation in the HTR1A gene and sudden infant death syndrome
Megan E Morley, Casey M Rand, Elizabeth M Berry-Kravis, et al.
American Journal on Intellectual and Developmental Disabilities
|
December 22, 2022
FMR1 CGG Repeats and Stress Influence Self-Reported Cognitive Functioning in Mothers
Nell Maltman, Leann Smith DaWalt, Jinkuk Hong, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2003
Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis
Debra E Weese-Mayer, Lili Zhou, Elizabeth M Berry-Kravis, et al.
American Journal of Medical Genetics. Part A
|
June 10, 2006
Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome
Casey M Rand, Debra E Weese-Mayer, Brion S Maher, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 86) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics. Part A
|
September 21, 2016
Importance of a specialty clinic for individuals with fragile X syndrome
Jeannie Visootsak, Sharon A Kidd, Tovi Anderson, et al.
Pediatric Pulmonology
|
December 5, 2009
Congenital central hypoventilation syndrome: neurocognitive functioning in school age children
Frank A Zelko, Michael N Nelson, Sue E Leurgans, et al.
American Journal on Intellectual and Developmental Disabilities
|
October 27, 2025
FMR1 Premutation Carrier Mothers' Daily Negative Affect and Cortisol: Probing the Impacts of Stress Exposure, Coping Style, and CGG Repeats
Leann Smith DaWalt, Jinkuk Hong, Catherine Rogers Gaspar, et al.
American Journal of Medical Genetics. Part A
|
May 13, 2006
3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis
Brion S Maher, Mary L Marazita, Casey Rand, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 9, 2010
An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management
Debra E Weese-Mayer, Elizabeth M Berry-Kravis, Isabella Ceccherini, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
November 6, 2010
Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers
Lawrence J Jennings, Min Yu, Lili Zhou, et al.
American Journal of Medical Genetics. Part A
|
February 21, 2008
Genetic variation in the HTR1A gene and sudden infant death syndrome
Megan E Morley, Casey M Rand, Elizabeth M Berry-Kravis, et al.
American Journal on Intellectual and Developmental Disabilities
|
December 22, 2022
FMR1 CGG Repeats and Stress Influence Self-Reported Cognitive Functioning in Mothers
Nell Maltman, Leann Smith DaWalt, Jinkuk Hong, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2003
Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis
Debra E Weese-Mayer, Lili Zhou, Elizabeth M Berry-Kravis, et al.
American Journal of Medical Genetics. Part A
|
June 10, 2006
Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome
Casey M Rand, Debra E Weese-Mayer, Brion S Maher, et al.
Page
of 9