Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation

P. Vestergaard,; J.P. Kroustrup,; H. Rønne,; C. Eng,; P. Laurberg,

doi:10.1515/IJDHD.1999.1.1.33

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Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation

P. Vestergaard, , J.P. Kroustrup, , H. Rønne, , C. Eng, und P. Laurberg,

Veröffentlicht/Copyright: 1. Januar 1999

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Aus der Zeitschrift International Journal on Disability and Human Development Band 1 Heft 1

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Chicago
Vancouver

Vestergaard,, P., Kroustrup,, J.P., Rønne,, H., Eng,, C. and Laurberg,, P.. "Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation" International Journal on Disability and Human Development, vol. 1, no. 1, pp. 33-38. https://doi.org/10.1515/IJDHD.1999.1.1.33

Vestergaard,, P., Kroustrup,, J., Rønne,, H., Eng,, C. & Laurberg,, P. (). Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation. International Journal on Disability and Human Development, 1(1), 33-38. https://doi.org/10.1515/IJDHD.1999.1.1.33

Vestergaard,, P., Kroustrup,, J., Rønne,, H., Eng,, C. and Laurberg,, P. () Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation. International Journal on Disability and Human Development, Vol. 1 (Issue 1), pp. 33-38. https://doi.org/10.1515/IJDHD.1999.1.1.33

Vestergaard,, P., Kroustrup,, J.P., Rønne,, H., Eng,, C. and Laurberg,, P.. "Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation" International Journal on Disability and Human Development 1, no. 1 (): 33-38. https://doi.org/10.1515/IJDHD.1999.1.1.33

Vestergaard, P, Kroustrup, J, Rønne, H, Eng, C, Laurberg, P. Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation. International Journal on Disability and Human Development. ;1(1): 33-38. https://doi.org/10.1515/IJDHD.1999.1.1.33

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Published Online: 1999-01

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Artikel in diesem Heft

CONTENTS
Letter from the Editors
The Human Genome Project, Positional Cloning of Inherited Disease Genes, and Multiple Endocrine Neoplasia Type 1
The "Little People" of the Island of Krk - Revisited. Etiology of Hypopituitarism Revealed
Further Delineation of Spondyloepimetaphyseal Dysplasia Shohat Type, and a Review of the Literature
Genetic Analyses of a Family with Familial Medullary and Papillary Thyroid Carcinoma
Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation
Germline V804M Mutation in the RET Proto-oncogene in Two Apparently Sporadic Cases of MTC Presenting in the Seventh Decade of Life
Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature
Non-Classical Congenital Adrenal Hyperplasia Phenotype in a Female Newborn Heterozygous for the 21-Hydroxylase Gene Mutation
BOOK REVIEWS. CALENDAR

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https://doi.org/10.1515/IJDHD.1999.1.1.33

Artikel in diesem Heft

CONTENTS
Letter from the Editors
The Human Genome Project, Positional Cloning of Inherited Disease Genes, and Multiple Endocrine Neoplasia Type 1
The "Little People" of the Island of Krk - Revisited. Etiology of Hypopituitarism Revealed
Further Delineation of Spondyloepimetaphyseal Dysplasia Shohat Type, and a Review of the Literature
Genetic Analyses of a Family with Familial Medullary and Papillary Thyroid Carcinoma
Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation
Germline V804M Mutation in the RET Proto-oncogene in Two Apparently Sporadic Cases of MTC Presenting in the Seventh Decade of Life
Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature
Non-Classical Congenital Adrenal Hyperplasia Phenotype in a Female Newborn Heterozygous for the 21-Hydroxylase Gene Mutation
BOOK REVIEWS. CALENDAR