De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair

H. Hampel,; C.M. Allen,; S.D. Chernausek,; T.W. Prior,; C. Eng,

doi:10.1515/IJDHD.2000.1.3.143

Home De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair

Article

Licensed

Unlicensed Requires Authentication

De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair

H. Hampel, , C.M. Allen, , S.D. Chernausek, , T.W. Prior, and C. Eng,

Published/Copyright: July 1, 2000

Published by

Become an author with De Gruyter Brill

Author Information Explore this Subject

From the journal International Journal on Disability and Human Development Volume 1 Issue 3

MLA
APA
Harvard
Chicago
Vancouver

MLA
APA
Harvard
Chicago
Vancouver

Hampel,, H., Allen,, C.M., Chernausek,, S.D., Prior,, T.W. and Eng,, C.. "De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair" International Journal on Disability and Human Development, vol. 1, no. 3, pp. 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel,, H., Allen,, C., Chernausek,, S., Prior,, T. & Eng,, C. (). De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair. International Journal on Disability and Human Development, 1(3), 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel,, H., Allen,, C., Chernausek,, S., Prior,, T. and Eng,, C. () De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair. International Journal on Disability and Human Development, Vol. 1 (Issue 3), pp. 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel,, H., Allen,, C.M., Chernausek,, S.D., Prior,, T.W. and Eng,, C.. "De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair" International Journal on Disability and Human Development 1, no. 3 (): 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Hampel, H, Allen, C, Chernausek, S, Prior, T, Eng, C. De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair. International Journal on Disability and Human Development. ;1(3): 143-148. https://doi.org/10.1515/IJDHD.2000.1.3.143

Copy

Copied to clipboard

BibTeX EndNote RIS

Published Online: 2000-07

You are currently not able to access this content.

Articles in the same Issue

CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR

Search journal Search the content of this journal

https://doi.org/10.1515/IJDHD.2000.1.3.143

Articles in the same Issue

CONTENTS
Letter from the Editors
Prader-Willi and Angelman Syndromes: Diagnostic Approach
Argl83His, a New Mutational "Hot-Spot" in the Growth Hormone Gene
Novel Mutation (Arg836ter) of the Sulfonylurea Receptor-1 (SUR1) Gene in Congenital Hyperinsulinism
De novo RET Mutation Positive Multiple Endocrine Neoplasia Type 2B and Hereditary Nonpolyposis Colorectal Cancer Syndrome Occurring in the Same Family: Parent-of-Origin and Mismatch Repair
Bromocriptine Resistant Prolactinomas and Non-Functioning Pituitary Tumors: Somatic Mutational Analyses of the Dopamine Type 2 Receptor and the MEN1 Gene
Genetic Studies in Familial Aldosteronism Not Suppressible by Dexamethasone
Recombination Between the Sodium Channel SCN8A and the Allgrove Syndrome Gene in a Puerto Rican Kindred
BOOK REVIEWS. CALENDAR