Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype

W. Zumkeller,; P. Wieacker,

doi:10.1515/IJDHD.2001.2.3.141

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Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype

W. Zumkeller, und P. Wieacker,

Veröffentlicht/Copyright: 1. Juli 2001

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Aus der Zeitschrift International Journal on Disability and Human Development Band 2 Heft 3

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Zumkeller,, W. and Wieacker,, P.. "Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype" International Journal on Disability and Human Development, vol. 2, no. 3, pp. 141-150. https://doi.org/10.1515/IJDHD.2001.2.3.141

Zumkeller,, W. & Wieacker,, P. (). Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype. International Journal on Disability and Human Development, 2(3), 141-150. https://doi.org/10.1515/IJDHD.2001.2.3.141

Zumkeller,, W. and Wieacker,, P. () Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype. International Journal on Disability and Human Development, Vol. 2 (Issue 3), pp. 141-150. https://doi.org/10.1515/IJDHD.2001.2.3.141

Zumkeller,, W. and Wieacker,, P.. "Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype" International Journal on Disability and Human Development 2, no. 3 (): 141-150. https://doi.org/10.1515/IJDHD.2001.2.3.141

Zumkeller, W, Wieacker, P. Short Stature Homeobox-Containing Gene (SHOX): Genotype and Phenotype. International Journal on Disability and Human Development. ;2(3): 141-150. https://doi.org/10.1515/IJDHD.2001.2.3.141

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Published Online: 2001-07

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Artikel in diesem Heft

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

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https://doi.org/10.1515/IJDHD.2001.2.3.141

Artikel in diesem Heft

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