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American Journal of Medical Genetics|August 1, 1989
Pectoralis major defect and Poland sequence in second cousins: extension of the Poland sequence spectrumF C Fraser, G M Ronen, E O'LearyBirth Defects Original Article Series|June 1, 1971
Familial holoprosencephalyL Dallaire, F C Fraser, F W WiglesworthAmerican Journal of Medical Genetics|January 16, 1995
Nutritional patterns of mothers of children with neural tube defects in NewfoundlandJ K Friel, M Frecker, F C FraserAmerican Journal of Diseases of Children (1960)|December 1, 1976
A spinal arteriovenous malformation with hereditary cutaneous hemangiomasP Kaplan, R D Hollenberg, F C FraserAmerican Journal of Medical Genetics|January 1, 1980
Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing lossF C Fraser, J R Sproule, F HalalClinical Endocrinology|December 1, 1985
A prognostic score for Graves' diseaseM Preus, M F Frecker, V Stenszky, et al.Clinical Genetics|July 1, 1985
Possible teratogenic effects of artificial insemination by donorR A Forse, C F Ackman, F C FraserObstetrics and Gynecology|January 1, 1978
Inidcations for prenatal diagnosis in relatives of patients with neural tube defectsA Lippman-Hand, F C Fraser, C J BiddleClinical Genetics|April 1, 1995
Familial hypertryptophanemia in two siblingsJ R Martin, C S Mellor, F C FraserAmerican Journal of Medical Genetics|March 1, 1983
Autosomal dominant duplication of the renal collecting system, hearing loss, and external ear anomalies: a new syndrome?F C Fraser, S Aymé, F Halal, et al.Pageof 10