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The Medical Journal of Australia|August 7, 1989
Analysis of DNA probes for the prenatal diagnosis of cystic fibrosisP J Dry, S Wake, C F Robertson, et al.Clinical Genetics|February 3, 2006
Predictive genetic testing in young people for adult-onset conditions: where is the empirical evidence?R E Duncan, M B DelatyckiCurrent Opinion in Molecular Therapeutics|January 24, 2002
Strategies to find new genes involved in drug metabolismL J SheffieldAmerican Journal of Medical Genetics|February 6, 1999
Persistent truncus arteriosus in monozygotic twins: case report and literature reviewC Mas, M B Delatycki, R G WeintraubClinical Genetics|November 15, 2002
Sleep disturbance in mucopolysaccharidosis type III (Sanfilippo syndrome): a survey of managing cliniciansJ Fraser, J E Wraith, M B DelatyckiJournal of Medical Genetics|January 14, 2000
Friedreich ataxia: an overviewM B Delatycki, R Williamson, S M ForrestThe Medical Journal of Australia|August 19, 1985
The creation of therapeutic orphans--or, what have we learnt from the Debendox fiasco?L J Sheffield, R BatagolPrenatal Diagnosis|March 4, 1998
Trisomy 13 mosaicism at prenatal diagnosis: dilemmas in interpretationM B Delatycki, M D Pertile, R J GardnerAmerican Journal of Medical Genetics|June 1, 1986
Distal arthrogryposis type II: a family with varying congenital abnormalitiesJ A Reiss, L J SheffieldAmerican Journal of Medical Genetics|February 15, 2001
New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafnessD J Amor, M B Delatycki, R J Gardner, et al.Pageof 662