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Journal of Medical Genetics|August 1, 1989
Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of WalesL A Tyfield, A L Meredith, M J Osborn, et al.
Archives of Disease in Childhood|July 1, 1979
Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated casesJ R Sibert, P S Harper, R J Thompson, et al.
Journal of Medical Genetics|April 1, 1990
Becker muscular dystrophy: correlation of deletion type with clinical severityA M Norman, N S Thomas, H M Kingston, et al.
Clinical Genetics|January 1, 1995
Risk estimates for developing motor neurone disease in first-degree relativesC M James, R G Newcombe, P S Harper, et al.
Archives of Disease in Childhood|June 1, 1989
Early diagnosis and secondary prevention of Duchenne muscular dystrophyR A Smith, J R Sibert, S J Wallace, et al.
Journal of Medical Genetics|June 1, 1977
Genetic study of Welsh gypsiesE M Williams, P R Harper
British Journal of Pharmacology|August 1, 1973
Further studies regarding the structure activity relationships of beta-adrenoceptor antagonistsE E Bagwell, E M Williams
The Journal of Laboratory and Clinical Medicine|May 1, 1978
Fibronectin concentration is decreased in plasma of severely ill patients with disseminated intravascular coagulationD F Mosher, E M Williams
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