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Journal of Cellular Biochemistry|June 16, 2007
COMP mutations: domain-dependent relationship between abnormal chondrocyte trafficking and clinical PSACH and MED phenotypesTung-Ling L Chen, Karen L Posey, Jacqueline T Hecht, et al.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.Faraday Discussions|March 29, 2001
Effect of the projected band gap on the formation of negative ions in grazing collisions from Cu surfacesT Hecht, H Winter, A G Borisov, et al.JAMA|November 12, 1982
Platelet transfusion therapy in an alloimmunized patient. The value of crossmatch procedures for donor selectionT Hecht, J L Wolf, L Mraz, et al.Acta Biologica Et Medica Germanica|January 1, 1978
[Learning and memory processes during postnatal ontogenesis in rats with spontaneous hypertension]K Hecht, M Poppei, T Hecht, et al.Urologia Internationalis|January 1, 1993
Nocturnal pollakiuria is a symptom of obstructive sleep apneaJ Krieger, C Petiau, E Sforza, 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.American Journal of Medical Genetics|December 18, 2001
A natural history of cleidocranial dysplasiaS C Cooper, C M Flaitz, D A Johnston, et al.American Journal of Medical Genetics. Part A|September 21, 2007
Mortality in achondroplasia study: a 42-year follow-upJulia Wynn, Terri M King, Michael J Gambello, et al.Pageof 34