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American Journal of Medical Genetics|April 24, 1996
A split hand-split foot (SHFM3) gene is located at 10q24-->25F Gurrieri, P Prinos, D Tackels, et al.American Journal of Medical Genetics|June 1, 1991
Beemer-Langer syndrome with manifestations of an orofaciodigital syndromeA E Lin, N Doshi, L Flom, et al.American Journal of Diseases of Children (1960)|September 1, 1987
The pattern of cardiovascular malformation in the CHARGE associationA E Lin, A J Chin, W Devine, et al.Journal of the American College of Cardiology|March 1, 1986
Subaortic obstruction in complex congenital heart disease: management by proximal pulmonary artery to ascending aorta end to side anastomosisA E Lin, H Laks, G Barber, et al.American Journal of Medical Genetics|October 23, 1997
Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolismH Menger, A E Lin, H V Toriello, et al.Immunotargets and Therapy|May 27, 2026
Development of an Active Chimeric IL13Rα2 ADC for Diffuse Intrinsic Pontine GliomaXiaolei Lian, Victoria J Allanson, Samuel V Rasmussen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Heterotaxy: associated conditions and hospital-based prevalence in newbornsA E Lin, B S Ticho, K Houde, et al.American Journal of Medical Genetics|January 31, 1997
Cardiovascular malformations in Smith-Lemli-Opitz syndromeA E Lin, H H Ardinger, R H Ardinger, et al.American Journal of Medical Genetics|February 15, 1993
Further delineation of the Baller-Gerold syndromeA E Lin, E McPherson, N A Nwokoro, et al.Clinical Genetics|April 1, 1986
Congenital heart disease in supernumerary der(22),t(11;22) syndromeA E Lin, J Bernar, A J Chin, et al.Pageof 9