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Journal of Child Neurology|March 9, 2011
Pontocerebellar hypoplasia: review of classification and genetics, and exclusion of several genes known to be important for cerebellar developmentStephen M Maricich, Kaashif A Aqeeb, Yalda Moayedi, et al.Patient Education and Counseling|February 12, 2011
Examining risk perception among men with a family history of prostate cancerAndrew G Matthew, Christina Paradiso, Kristen L Currie, et al.Nature Structural & Molecular Biology|August 17, 2010
Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locusJohn D Cleary, Stéphanie Tomé, Arturo López Castel, et al.Depression and Anxiety|August 1, 2022
Risk of major malformations in infants after first-trimester exposure to benzodiazepines: Results from the Massachusetts General Hospital National Pregnancy Registry for Psychiatric MedicationsMercedes J Szpunar, Marlene P Freeman, Lauren A Kobylski, et al.Iscience|June 30, 2026
A digital microfluidic platform for cell-based non-invasive testingDylan Siriwardena, Michael D M Dryden, M Dean Chamberlain, et al.Blood|August 27, 2005
Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet alpha-granule biogenesisBryan Lo, Ling Li, Paul Gissen, et al.JACC. Heart Failure|July 16, 2014
Spectrum and outcome of primary cardiomyopathies diagnosed during fetal lifeRoland Weber, Paul Kantor, David Chitayat, et al.Prenatal Diagnosis|April 3, 2012
Referral patterns for microarray testing in prenatal diagnosisLisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, et al.Hypertension (Dallas, Tex. : 1979)|December 19, 2007
Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNASylvia Bähring, Martin Kann, Yvette Neuenfeld, et al.American Journal of Medical Genetics. Part A|May 16, 2012
Brain abnormalities in patients with Beckwith-Wiedemann syndromeKate Gardiner, David Chitayat, Sanaa Choufani, et al.Pageof 45