| Year |
Citation |
Score |
| 1991 |
Robb LJ, Fraser FC, Der Kaloustian VM. Treacher Collins-Franceschetti syndrome with tracheoesophageal fistula, rectovaginal fistula, and anal atresia: variant, or new syndrome? American Journal of Medical Genetics. 39: 119-20. PMID 1867255 DOI: 10.1002/Ajmg.1320390126 |
0.324 |
|
| 1990 |
Chen MF, Vekemans M, Meagher-Villemure K, Outerbridge E, Fraser FC, Der Kaloustian VM. Aminopterin-like syndrome sine aminopterin associated with translocation involving chromosomes 5 and 10. American Journal of Medical Genetics. 37: 478-81. PMID 2260592 DOI: 10.1002/Ajmg.1320370411 |
0.488 |
|
| 1989 |
Verloes A, Delfortrie J, Lambotte C, Fraser FC, Reynolds JF. 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. PMID 2705477 DOI: 10.1002/Ajmg.1320320104 |
0.329 |
|
| 1987 |
Küster W, Majewski F, Hammerstein W, Fraser FC, Preus M. Alopecia, macular degeneration, and growth retardation: a new syndrome? American Journal of Medical Genetics. 28: 477-481. PMID 3425621 DOI: 10.1002/Ajmg.1320280225 |
0.309 |
|
| 1985 |
Filippi G, Fraser FC, Perus M. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome? American Journal of Medical Genetics. 22: 821-824. PMID 4073130 DOI: 10.1002/Ajmg.1320220416 |
0.324 |
|
| 1982 |
Blaichman S, Fraser FC, Preus M. Tracheoesophageal fistula, protruding pinnae, proximal interphalangeal symphalangism of fifth finger. A new syndrome? American Journal of Medical Genetics. 13: 233-234. PMID 7137234 DOI: 10.1002/Ajmg.1320130215 |
0.311 |
|
| 1982 |
Vekemans M, Fraser FC. Susceptibility to cleft palate and the major histocompatibility complex (H-2) in the mouse. Teratology. 25: 267-70. PMID 7101203 DOI: 10.1002/tera.1420250216 |
0.402 |
|
| 1981 |
Vekemans M, Taylor BA, Fraser FC. 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. PMID 7333460 |
0.427 |
|
| 1980 |
Juriloff DM, Fraser FC. Genetic maternal effects on cleft lip frequency in A/J and CL/Fr mice. Teratology. 21: 167-75. PMID 7394720 DOI: 10.1002/Tera.1420210206 |
0.563 |
|
| 1979 |
Vekemans M, Fraser FC. Stage of palate closure as one indication of "liability" to cleft palate. American Journal of Medical Genetics. 4: 95-102. PMID 495657 DOI: 10.1002/ajmg.1320040111 |
0.424 |
|
| 1976 |
Kaplan P, Cummings C, Fraser FC. A "community" of face-limb malformation syndromes The Journal of Pediatrics. 89: 241-247. PMID 940017 DOI: 10.1016/S0022-3476(76)80456-8 |
0.324 |
|
| 1975 |
Berman P, Desjardins C, Fraser FC. The inheritance of the Aarskog facial-digital-genital syndrome. The Journal of Pediatrics. 86: 885-91. PMID 1127528 DOI: 10.1016/S0022-3476(75)80219-8 |
0.316 |
|
| 1974 |
MacLeod PM, Fraser FC. Congenital contractural arachnodactyly. A heritable disorder of connective tissue distinct from Marfan syndrome. American Journal of Diseases of Children (1960). 126: 810-2. PMID 4759368 DOI: 10.1001/Archpedi.1973.02110190652014 |
0.309 |
|
| 1974 |
Levy EP, Fletcher BD, Fraser FC. Mohr syndrome with subclinical expression of the bifid great toe. American Journal of Diseases of Children (1960). 128: 531-3. PMID 4414705 DOI: 10.1001/Archpedi.1974.02110290101019 |
0.321 |
|
| 1973 |
Preus M, Fraser FC. Dermatoglyphics and syndromes. American Journal of Diseases of Children (1960). 124: 933-43. PMID 4265019 DOI: 10.1001/Archpedi.1972.02110180135022 |
0.343 |
|
| 1946 |
STEINBERG AG, FRASER FC. The expression and interaction of hereditary factors affecting hair growth in mice; external observations. Canadian Journal of Research. 24: 1-9. PMID 21066139 |
0.46 |
|
| 1944 |
Steinberg AG, Fraser FC. Studies on the Effect of X Chromosome Inversions on Crossing over in the Third Chromosome of Drosophila Melanogaster. Genetics. 29: 83-103. PMID 17247110 |
0.462 |
|
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