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Nature Genetics|July 1, 1995
Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiaJ T Hecht, L D Nelson, E Crowder, et al.
Journal of Molecular and Cellular Cardiology|February 9, 2025
Autoinhibition of cMyBP-C by its middle domainsAngela C Greenman, Rachel L Sadler, Samantha P Harris
The American Surgeon|February 1, 1991
Axillary subclavian vein thrombosis. Changing patterns of etiology, diagnostic, and therapeutic modalitiesA F Aburahma, D L Sadler, P A Robinson
American Journal of Medical Genetics|November 1, 1991
Cognitive and motor skills in achondroplastic infants: neurologic and respiratory correlatesJ T Hecht, N M Thompson, T Weir, et al.
Journal of Dental Research|May 7, 2014
Functional Significance of MMP3 and TIMP2 Polymorphisms in Cleft Lip/PalateA Letra, M Zhao, R M Silva, et al.
Prenatal Diagnosis|August 1, 1997
Recurrent severe infantile cortical hyperostosis (Caffey disease) in siblingsB M Drinkwater, J P Crino, J Garcia, et al.
Journal of Developmental Origins of Health and Disease|August 21, 2014
Pregnancy and neonatal outcomes following hyperemesis gravidarumR L Coetzee, B Cormack, L Sadler, et al.
Joint Commission Journal on Quality and Patient Safety|January 5, 2008
The role of the physical environment in crossing the quality chasmKerm Henriksen, Sandi Isaacson, Blair L Sadler, et al.
American Journal of Medical Genetics|December 18, 2001
A natural history of cleidocranial dysplasiaS C Cooper, C M Flaitz, D A Johnston, et al.
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