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Schweizerische Medizinische Wochenschrift|November 7, 2000
Registration of congenital anomalies in Switzerland by EUROCATM C Addor, G Pescia, D F SchorderetRevue Neurologique|June 1, 1996
[Familial hyperekplexia: startle disease. Clinical, electrophysiological and genetic study of a family]A Bernasconi, F Regli, D F Schorderet, et al.Praxis|August 27, 1996
[Retinoblastoma: clinical and molecular diagnostic aspects]F Thonney, F L Munier, A Balmer, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A new case of Pfeiffer syndrome with mutation in FGFR2M C Addor, F Gudinchet, R N Laurini, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 14, 1997
Frequency and impact of autosomal dominant polycystic kidney disease in the Seychelles (Indian Ocean)C Yersin, P Bovet, J P Wauters, et al.Klinische Monatsblatter Fur Augenheilkunde|May 1, 1996
Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counselingF L Munier, F Thonney, A Balmer, et al.Nature Genetics|March 1, 1997
Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesF L Munier, E Korvatska, A Djemaï, et al.Schweizerische Rundschau Fur Medizin Praxis = Revue Suisse De Medecine Praxis|May 17, 1994
[Polymerase chain reaction: basic principles]D F SchorderetAmerican Journal of Medical Genetics|June 1, 1991
Using OMIM (On-line Mendelian Inheritance in Man) as an expert system in medical geneticsD F SchorderetPageof 14