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Brain : a Journal of Neurology|November 18, 2021
Sensory processing dysregulations as reliable translational biomarkers in SYNGAP1 haploinsufficiencyMaria Isabel Carreño-Muñoz, Bidisha Chattopadhyaya, Kristian Agbogba, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 14, 2019
Efficacy and safety of hydrolyzed rice-protein formulas for the treatment of cow's milk protein allergyA Bocquet, C Dupont, J-P Chouraqui, et al.
Journal of Visceral Surgery|December 30, 2015
Esophageal tissue engineering: Current status and perspectivesT Poghosyan, J Catry, M Luong-Nguyen, et al.
Cardiology in the Young|April 6, 2012
Risk of congenital heart defects is influenced by genetic variation in folate metabolismKaren E Christensen, Yassamin Feroz Zada, Charles V Rohlicek, et al.
Human Genetics|December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13G B Collin, J D Marshall, C F Boerkoel, et al.
Journal of the American Heart Association|November 26, 2025
Association Between Monoclonal Gammopathy of Undetermined Significance and Cardiovascular Disease Risk: A Veterans Health Administration StudyTzeyu L Michaud, Mei Wang, Daphne R Friedman, et al.
Clinical Genetics|May 2, 2015
A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephalyM Srour, F F Hamdan, Z Gan-Or, et al.
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