Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature

A. Pathomvanich,; C.C. Koch,; C.A. Stratakis,

doi:10.1515/IJDHD.1999.1.1.47

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Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature

A. Pathomvanich, , C.C. Koch, und C.A. Stratakis,

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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Pathomvanich,, A., Koch,, C.C. and Stratakis,, C.A.. "Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature" International Journal on Disability and Human Development, vol. 1, no. 1, pp. 47-50. https://doi.org/10.1515/IJDHD.1999.1.1.47

Pathomvanich,, A., Koch,, C. & Stratakis,, C. (). Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature. International Journal on Disability and Human Development, 1(1), 47-50. https://doi.org/10.1515/IJDHD.1999.1.1.47

Pathomvanich,, A., Koch,, C. and Stratakis,, C. () Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature. International Journal on Disability and Human Development, Vol. 1 (Issue 1), pp. 47-50. https://doi.org/10.1515/IJDHD.1999.1.1.47

Pathomvanich,, A., Koch,, C.C. and Stratakis,, C.A.. "Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature" International Journal on Disability and Human Development 1, no. 1 (): 47-50. https://doi.org/10.1515/IJDHD.1999.1.1.47

Pathomvanich, A, Koch, C, Stratakis, C. Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature. International Journal on Disability and Human Development. ;1(1): 47-50. https://doi.org/10.1515/IJDHD.1999.1.1.47

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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.1999.1.1.47

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