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Prenatal Diagnosis|March 1, 1986
First trimester monitoring of a pregnancy at risk for glucose phosphate isomerase deficiencyB Dallapiccola, G Novelli, G Ferranti, et al.Human Genetics|September 10, 1999
CTG repeats distribution and Alu insertion polymorphism at myotonic dystrophy (DM) gene in Amhara and Oromo populations of EthiopiaM Gennarelli, M Pavoni, F Cruciani, et al.Mutation Research|July 24, 2001
Three novel mutations causing a truncated protein within the RP2 gene in Italian families with X-linked retinitis pigmentosaA De Luca, I Torrente, M Mangino, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome (deletion 22q11.2 syndrome)M C Digilio, B Marino, M Cappa, et al.British Journal of Audiology|July 13, 2000
Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome)M C Digilio, C Pacifico, L Tieri, et al.American Journal of Medical Genetics|May 26, 1999
Cardiac malformations in patients with oral-facial-skeletal syndromes: clinical similarities with heterotaxiaM C Digilio, B Marino, A Ammirati, et al.Cancer Genetics and Cytogenetics|November 1, 1981
Chromosome pattern, occupation, and clinical features in patients with acute nonlymphocytic leukemiaF Mitelman, P G Nilsson, L Brandt, et al.Helvetica Paediatrica Acta|May 1, 1983
Beta-cell function assessed by plasma C-peptide evaluation in diabetic thalassaemic patientsG Atti, L Capra, V De Sanctis, et al.Journal of Food Protection|July 7, 2007
Inactivation of calcium-dependent lactic acid bacteria phages by phosphatesV B Suárez, M L Capra, M Rivera, et al.Genomics|January 25, 2000
Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndromeA Botta, F Sangiuolo, L Calza, et al.Pageof 34