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Clinical Genetics|April 1, 1995
Familial hypertryptophanemia in two siblingsJ R Martin, C S Mellor, F C FraserClinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1983
Familial hypertryptophanemia, tryptophanuria and indoleketonuriaW Snedden, C S Mellor, J R MartinThe British Journal of Psychiatry : the Journal of Mental Science|April 1, 1992
Dermatoglyphic evidence of fluctuating asymmetry in schizophreniaC S MellorCanadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|January 1, 1981
Genetics society of Canada award of excellence lecture. The genetics of common familial disorders--major genes or multifactorial?F C FraserCanadian Medical Association Journal|December 1, 1982
Diazepam withdrawal syndrome: its prolonged and changing natureC S Mellor, V K JainAmerican Journal of Medical Genetics|January 1, 1981
Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly"F C Fraser, A LytwynJournal of Medical Genetics|December 1, 1982
Spectrum of anomalies in Fanconi anaemiaA Glanz, F C FraserAmerican Journal of Medical Genetics|March 4, 2000
Recurrence risk for sibs of children with "sporadic" achondroplasiaG Mettler, F C FraserPageof 29