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Developmental Medicine and Child Neurology|July 1, 1996
X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one familyC M Brewer, B J Fredericks, J M Pont, et al.Neuropediatrics|June 1, 1997
Batten disease in the west of Scotland 1974-1995 including five cases of the juvenile form with granular osmiophilic depositsY J Crow, J L Tolmie, A G Howatson, et al.American Journal of Medical Genetics|June 1, 1987
Genetic aspects of early childhood scoliosisJ M Connor, A N Conner, R A Connor, et al.Journal of Medical Genetics|May 1, 1990
Restrictive dermopathy: a report of three casesQ Mok, R Curley, J L Tolmie, et al.Journal of Medical Genetics|February 1, 1995
The prenatal exclusion test for Huntington's disease: experience in the west of Scotland, 1986-1993J L Tolmie, H R Davidson, H M May, et al.The British Journal of Ophthalmology|June 1, 1997
A novel pattern of oculocerebral malformationB J Clark, W R Lee, D Doyle, et al.Nature Biotechnology|March 7, 2001
Large-scale analysis of the yeast proteome by multidimensional protein identification technologyM P Washburn, D Wolters, J R YatesHuman Genetics|February 1, 1996
Clonality of tuberous sclerosis harmatomas shown by non-random X-chromosome inactivationA J Green, T Sepp, J R YatesNature Genetics|February 1, 1994
Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patientsA J Green, M Smith, J R YatesJournal of Medical Genetics|November 1, 1996
Loss of heterozygosity in tuberous sclerosis hamartomasT Sepp, J R Yates, A J GreenPageof 56