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American Journal of Human Genetics|August 1, 1992
The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, P Lunt, M Sarfarazi, et al.Journal of Medical Genetics|March 2, 1999
Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat lengthP Kehoe, M Krawczak, P S Harper, et al.Clinical and Experimental Immunology|January 1, 1980
Recurrent meningococcal infections associated with a functional deficiency of the C8 component of human complementN Matthews, J M Stark, P S Harper, et al.Prenatal Diagnosis|February 1, 1987
Lack of sampling site variation in chorion villus biopsy as assessed by DNA, enzymatic, morphological and cytogenetical analysesM Upadhyaya, B Jasani, E Little, et al.Journal of Medical Genetics|August 1, 1990
Exclusion testing in pregnancy for Huntington's diseaseA Tyler, O W Quarrell, L P Lazarou, et al.Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1M Upadhyaya, A Fryer, J MacMillan, et al.Clinical Genetics|June 1, 1990
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNAM Upadhyaya, R A Smith, N S Thomas, et al.Journal of Medical Genetics|August 1, 1982
A genetic register for Huntington's chorea in South WalesP S Harper, A Tyler, S Smith, et al.Archives of Disease in Childhood|July 1, 1989
Screening for Duchenne muscular dystrophyR A Smith, M Rogers, D M Bradley, et al.Genomics|December 1, 1987
Chromosome 17 markers and von Recklinghausen neurofibromatosis: a genetic linkage study in a British populationM Upadhyaya, M Sarfarazi, S M Huson, et al.Pageof 30