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Thorax|June 13, 1998
Familial primary spontaneous pneumothorax consistent with true autosomal dominant inheritanceP J Morrison, R C Lowry, N C NevinThe Ulster Medical Journal|October 1, 1993
Huntington disease in County Donegal: epidemiological trends over four decadesP J Morrison, N C NevinIrish Journal of Medical Science|May 1, 1994
Serum iron, total iron binding capacity and ferritin in early Huntington disease patientsP J Morrison, N C NevinJournal of Medical Genetics|September 1, 1996
Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome)P J Morrison, N C NevinAmerican Journal of Medical Genetics|March 1, 1992
Interstitial deletion 8p21.3----p23.1 in a 6-year-old girlP J Morrison, J Jones, N C NevinJournal of Medical Genetics|July 1, 1995
The epidemiology of Huntington's disease in Northern IrelandP J Morrison, W P Johnston, N C NevinJournal of Medical Genetics|December 1, 1993
Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern IrelandP J Morrison, C A Graham, N C NevinJournal of Medical Genetics|February 1, 1990
Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductaseN C Nevin, P J Morrison, J Jones, et al.American Journal of Medical Genetics|November 1, 1992
Cardiovascular abnormalities in the oculo-auriculo-vertebral spectrum (Goldenhar syndrome)P J Morrison, H C Mulholland, B G Craig, et al.Henry Ford Hospital Medical Journal|January 1, 1989
MEN 2A: update on the Northern Ireland and Australian familyP J Morrison, D R Hadden, C J Russell, et al.Pageof 23