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American Journal of Medical Genetics|November 15, 1993
Limb deficiencies, chorion villus sampling, and advanced maternal ageJ Halliday, J Lumley, L J Sheffield, et al.Journal of Neurology|October 14, 2009
A comparison of three measures of upper limb function in Friedreich ataxiaL A Corben, G Tai, C Wilson, et al.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.American Journal of Human Genetics|November 1, 1983
Regional localization for HLA by recombination with a fragile site at 6p23J C Mulley, J Hay, L J Sheffield, et al.Australian and New Zealand Journal of Medicine|April 1, 1996
Detection of carriers of haemophilia A: use of bioassays and restriction fragment length polymorphisms (RFLP)Z Rudzki, S E Rodgers, L J Sheffield, et al.The Medical Journal of Australia|May 20, 1991
Perceptions of genetic risk in individuals with a one in two chance of developing autosomal dominant polycystic kidney diseaseD Ravine, L R McGregor, R G Walker, et al.Clinical Dysmorphology|January 1, 1995
'Disorganization-like syndrome' with 47,XXY and unilateral narrowing of the common iliac arteryC G Woods, S Treleaven, F R Betheras, et al.The Journal of Pediatrics|December 1, 1976
Chondrodysplasia punctata-23 cases of a mild and relatively common varietyL J Sheffield, D M Danks, V Mayne, et al.Prenatal Diagnosis|September 22, 1998
Fetal outcome and maternal morbidity after early amniocentesisV R Collins, C Webley, L J Sheffield, 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.Pageof 662