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Clinical Genetics|February 1, 2005
Genetic susceptibility screening in schools: attitudes of the school community towards hereditary haemochromatosisA A Gason, M A Aitken, S A Metcalfe, et al.Clinical Genetics|November 6, 2012
To tell or not to tell - what to do about p.C282Y heterozygotes identified by HFE screeningM B Delatycki, M Wolthuizen, M A Aitken, 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 DelatyckiClinical Genetics|January 26, 2006
Educational outcomes of a workplace screening program for genetic susceptibility to hemochromatosisA E Nisselle, V R Collins, A A Gason, et al.Clinical Genetics|April 22, 2004
A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosisM B Delatycki, K J Allen, P Gow, et al.American 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 ForrestPrenatal 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|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 12