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Journal of Medical Genetics|February 1, 1993
The genetics of malignant hyperthermiaS P Ball, K J JohnsonJournal of Medical Genetics|July 1, 1993
Genetic risk: women's understanding of carrier risks in Duchenne muscular dystrophyE P Parsons, A J ClarkeJournal of Medical Genetics|July 1, 1993
'Inside-out', back-to-front: a model for clinical population genetic screeningD Shickle, I HarveyJournal of Medical Genetics|July 1, 1993
Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische NephrologieK Zerres, S Rudnik-Schöneborn, F DegetJournal of Medical Genetics|July 1, 1993
Facioscapulohumeral muscular dystrophy: aspects of genetic counselling, acceptance of preclinical diagnosis, and fitnessS Eggers, M R Passos-Bueno, M ZatzJournal of Medical Genetics|July 1, 1993
Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentationE Bocian, T Mazurczak, E Buława, et al.Journal of Medical Genetics|August 1, 1993
Is skewed X inactivation responsible for symptoms in female carriers for adrenoleucodystrophy?E Watkiss, T Webb, S BundeyJournal of Medical Genetics|August 1, 1993
The substitution of glycine 661 by arginine in type III collagen produces mutant molecules with different thermal stabilities and causes Ehlers-Danlos syndrome type IVA Richards, P Narcisi, J Lloyd, et al.Journal of Medical Genetics|August 1, 1993
Dominant carpotarsal osteochondromatosisP Maroteaux, M Le Merrer, H Bensahel, et al.Journal of Medical Genetics|September 1, 1993
Epidermal mosaicism and Blaschko's linesC Moss, S Larkins, M Stacey, et al.Pageof 649