F. Clarke Fraser
Affiliations: | McGill University, Montreal, QC, Canada |
Website:
https://publications.mcgill.ca/medenews/2015/01/08/in-memoriam-dr-f-clarke-fraser-1920-2014/Google:
"F. Clarke Fraser"Bio:
(1920 - 2014)
http://www.cdnmedhall.org/inductees/dr-f-clarke-fraser
http://www.cdnmedhall.org/saying-farewell-dr-f-clarke-fraser
http://ohhgp.pendari.com/files/a3dba2ec_a439_4f76_b9ed_511cf35de8eb.pdf
https://www.ccmg-ccgm.org/news-article-11/122-news/218-news-article-14.html
DOI: 10.1016%2Fj.ajhg.2015.06.008
https://www.worldcat.org/oclc/903142403
Parents
Sign in to add mentorArthur G. Steinberg | grad student | 1945 | McGill | |
(The expression and interaction of hereditary factors affecting hair growth in mice.) |
Children
Sign in to add traineeDiana M Juriloff | grad student | 1977 | McGill |
Michel Vekemans | grad student | 1981 | Montreal children's hospital and McGill University (Neurotree) |
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Publications
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Robb LJ, Fraser FC, Der Kaloustian VM. (1991) Treacher Collins-Franceschetti syndrome with tracheoesophageal fistula, rectovaginal fistula, and anal atresia: variant, or new syndrome? American Journal of Medical Genetics. 39: 119-20 |
Chen MF, Vekemans M, Meagher-Villemure K, et al. (1990) Aminopterin-like syndrome sine aminopterin associated with translocation involving chromosomes 5 and 10. American Journal of Medical Genetics. 37: 478-81 |
Verloes A, Delfortrie J, Lambotte C, et al. (1989) GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome. American Journal of Medical Genetics. 32: 15-18 |
Küster W, Majewski F, Hammerstein W, et al. (1987) Alopecia, macular degeneration, and growth retardation: a new syndrome? American Journal of Medical Genetics. 28: 477-481 |
Filippi G, Fraser FC, Perus M. (1985) Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome? American Journal of Medical Genetics. 22: 821-824 |
Blaichman S, Fraser FC, Preus M. (1982) Tracheoesophageal fistula, protruding pinnae, proximal interphalangeal symphalangism of fifth finger. A new syndrome? American Journal of Medical Genetics. 13: 233-234 |
Vekemans M, Fraser FC. (1982) Susceptibility to cleft palate and the major histocompatibility complex (H-2) in the mouse. Teratology. 25: 267-70 |
Vekemans M, Taylor BA, Fraser FC. (1981) The susceptibility to cortisone-induced cleft palate of recombinant inbred strains of mice: lack of association with the H-2 haplotype. Genetical Research. 38: 327-31 |
Juriloff DM, Fraser FC. (1980) Genetic maternal effects on cleft lip frequency in A/J and CL/Fr mice. Teratology. 21: 167-75 |
Vekemans M, Fraser FC. (1979) Stage of palate closure as one indication of "liability" to cleft palate. American Journal of Medical Genetics. 4: 95-102 |