Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?

K. Sweet,; E. Martin,; C. Eng,; M. Shah,

doi:10.1515/IJDHD.2001.2.3.161

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Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?

K. Sweet, , E. Martin, , C. Eng, and M. Shah,

Published/Copyright: July 1, 2001

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From the journal International Journal on Disability and Human Development Volume 2 Issue 3

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Harvard
Chicago
Vancouver

Sweet,, K., Martin,, E., Eng,, C. and Shah,, M.. "Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?" International Journal on Disability and Human Development, vol. 2, no. 3, pp. 161-168. https://doi.org/10.1515/IJDHD.2001.2.3.161

Sweet,, K., Martin,, E., Eng,, C. & Shah,, M. (). Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?. International Journal on Disability and Human Development, 2(3), 161-168. https://doi.org/10.1515/IJDHD.2001.2.3.161

Sweet,, K., Martin,, E., Eng,, C. and Shah,, M. () Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?. International Journal on Disability and Human Development, Vol. 2 (Issue 3), pp. 161-168. https://doi.org/10.1515/IJDHD.2001.2.3.161

Sweet,, K., Martin,, E., Eng,, C. and Shah,, M.. "Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?" International Journal on Disability and Human Development 2, no. 3 (): 161-168. https://doi.org/10.1515/IJDHD.2001.2.3.161

Sweet, K, Martin, E, Eng, C, Shah, M. Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?. International Journal on Disability and Human Development. ;2(3): 161-168. https://doi.org/10.1515/IJDHD.2001.2.3.161

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https://doi.org/10.1515/IJDHD.2001.2.3.161

Articles in the same Issue

CONTENTS
Letter from the Editors
An Endocrinologist's View of Genetic Disorders in Ancient Greece
Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype
Independent Duplication of the Growth Hormone Gene in Three Anthropoidean Lineages
Familial Basal Cell Carcinoma, Melanoma and Skin Hypersensitivity with GIST: A New Hereditary Neuroendocrine Syndrome Involving the SCF/KIT Pathway?
Cushing's Syndrome Caused by Primary Pigmented Adrenocortical Micronodular Dysplasia - A Familial Case
The Genetics of Diabetes Mellitus: An International Seminar
BOOK REVIEWS. CALENDAR