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American Journal of Medical Genetics. Part A|July 16, 2008
Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorderCatalina García-Nonell, Eugenia Rigau Ratera, Susan Harris, et al.
Endocrinology|April 18, 2013
Epitope recognition in HLA-DR3 transgenic mice immunized to TSH-R protein or peptidesHidefumi Inaba, Leonard Moise, William Martin, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|December 31, 2013
Foot and ankle joint movements inside orthoses for children with spastic CPXue-Cheng Liu, David Embrey, Channing Tassone, et al.
Human Molecular Genetics|January 28, 2014
CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat sizeAnna Lisa Ludwig, Glenda M Espinal, Dalyir I Pretto, et al.
Molecular Therapy. Nucleic Acids|June 13, 2024
LNA-i-miR-221 activity in colorectal cancer: A reverse translational investigationAsad Ali, Katia Grillone, Serena Ascrizzi, et al.
Clinicoeconomics and Outcomes Research : CEOR|March 9, 2026
The Economic Impact of Loss to Follow-Up in Eosinophilic Esophagitis: A Model-Based Analysis from the Perspective of Italian National Health ServiceMarzia Bonfanti, Martina Fardella, Marianna Morani, et al.
American Journal of Medical Genetics. Part A|May 15, 2008
Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 geneEdmund C Jenkins, Flora Tassone, Lingling Ye, et al.
International Journal of Molecular Sciences|April 17, 2025
In Utero Alcohol and Unsuitable Home Environmental Exposure Combined with FMR1 Full Mutation Allele Cause Severe Fragile X Syndrome PhenotypesTri Indah Winarni, Ramkumar Aishworiya, Hannah Culpepper, et al.
Clinical Genetics|February 5, 2013
Prevalence and risk of migraine headaches in adult fragile X premutation carriersJ Au, R S Akins, L Berkowitz-Sutherland, et al.
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