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The Nebraska Medical Journal
|
May 1, 1993
A questionnaire survey of Midwest dermatologists on the clinical-genetic aspects of patients with multiple atypical nevi
R M Fusaro, L R Johnsen, R H Hoden, et al.
Journal of Medical Genetics
|
June 1, 1982
Leser-Trelat sign in mother and daughter with breast cancer
H T Lynch, R M Fusaro, J A Pester, et al.
British Journal of Cancer
|
June 1, 1990
Systemic cancer and the FAMMM syndrome
W Bergman, P Watson, J de Jong, et al.
Computers and Biomedical Research, an International Journal
|
February 11, 1998
Automated detection of hereditary syndromes using data mining
S Evans, S J Lemon, C A Deters, et al.
Archives of Dermatology
|
July 1, 1985
Eosinophilic cellulitis (Wells' syndrome)
M J Horn, D A Katz, C Bewtra, et al.
Pediatric Dermatology
|
July 1, 1985
The cutaneous evolution of nevi in a patient with familial, atypical, multiple-mole melanoma syndrome
H T Lynch, R M Fusaro, C L Treger, et al.
The British Journal of Dermatology
|
September 1, 1985
Muir-Torre syndrome in several members of a family with a variant of the Cancer Family Syndrome
H T Lynch, R M Fusaro, L Roberts, et al.
Cancer Genetics and Cytogenetics
|
April 1, 1983
A review of hereditary malignant melanoma including biomarkers in familial atypical multiple mole melanoma syndrome
H T Lynch, R M Fusaro, B S Danes, et al.
Journal of Medical Genetics
|
October 1, 1983
Familial atypical multiple mole-melanoma (FAMMM) syndrome: segregation analysis
H T Lynch, R M Fusaro, W J Kimberling, et al.
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education
|
January 1, 1993
The clinical use of genealogical techniques in cancer investigations: a questionnaire survey
R M Fusaro, R H Hoden, L R Johnsen, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 130) with videos related to
Sort By:
Page
of 13
The Nebraska Medical Journal
|
May 1, 1993
A questionnaire survey of Midwest dermatologists on the clinical-genetic aspects of patients with multiple atypical nevi
R M Fusaro, L R Johnsen, R H Hoden, et al.
Journal of Medical Genetics
|
June 1, 1982
Leser-Trelat sign in mother and daughter with breast cancer
H T Lynch, R M Fusaro, J A Pester, et al.
British Journal of Cancer
|
June 1, 1990
Systemic cancer and the FAMMM syndrome
W Bergman, P Watson, J de Jong, et al.
Computers and Biomedical Research, an International Journal
|
February 11, 1998
Automated detection of hereditary syndromes using data mining
S Evans, S J Lemon, C A Deters, et al.
Archives of Dermatology
|
July 1, 1985
Eosinophilic cellulitis (Wells' syndrome)
M J Horn, D A Katz, C Bewtra, et al.
Pediatric Dermatology
|
July 1, 1985
The cutaneous evolution of nevi in a patient with familial, atypical, multiple-mole melanoma syndrome
H T Lynch, R M Fusaro, C L Treger, et al.
The British Journal of Dermatology
|
September 1, 1985
Muir-Torre syndrome in several members of a family with a variant of the Cancer Family Syndrome
H T Lynch, R M Fusaro, L Roberts, et al.
Cancer Genetics and Cytogenetics
|
April 1, 1983
A review of hereditary malignant melanoma including biomarkers in familial atypical multiple mole melanoma syndrome
H T Lynch, R M Fusaro, B S Danes, et al.
Journal of Medical Genetics
|
October 1, 1983
Familial atypical multiple mole-melanoma (FAMMM) syndrome: segregation analysis
H T Lynch, R M Fusaro, W J Kimberling, et al.
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education
|
January 1, 1993
The clinical use of genealogical techniques in cancer investigations: a questionnaire survey
R M Fusaro, R H Hoden, L R Johnsen, et al.
Page
of 13