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The Journal of Molecular Diagnostics : JMD|May 14, 2013
Molecular inversion probe array for the genetic evaluation of stillbirth using formalin-fixed, paraffin-embedded tissueLeslie R Rowe, Harshwardhan M Thaker, John M Opitz, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|May 6, 2003
5-HT1A responsivity in patients with panic disorder before and after treatment with aerobic exercise, clomipramine or placeboAndreas Broocks, T Meyer, M Opitz, et al.American Journal of Medical Genetics|May 1, 1983
Brachymesomelia-renal syndromeL O Langer, R Nishino, A Yamaguchi, et al.Birth Defects Original Article Series|January 1, 1977
The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemiaC H Gonzalez, M V Durkin-Stamm, N F Geimer, et al.American Journal of Medical Genetics. Part A|October 15, 2013
Elements of morphology: general terms for congenital anomaliesRaoul C Hennekam, Leslie G Biesecker, Judith E Allanson, et al.Nature Methods|July 25, 2017
Rapidly inducible Cas9 and DSB-ddPCR to probe editing kineticsJohn C Rose, Jason J Stephany, William J Valente, et al.The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.American Journal of Medical Genetics|May 1, 1983
The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971C S Houston, J M Opitz, J W Spranger, et al.Cardiovascular and Interventional Radiology|June 29, 2026
Safety and Effectiveness in 400 Image-Guided Spleen Biopsies from the DeGIR RegistryR Ocker-Serger, M Opitz, L Klüner, et al.American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatmentF Lalatta, D Clerici Bagozzi, M G Salmoiraghi, et al.Pageof 34