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

W. Zumkeller,; P. Wieacker,

doi:10.1515/IJDHD.2001.2.3.141

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

Article

Licensed

Unlicensed Requires Authentication

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

W. Zumkeller, and P. Wieacker,

Published/Copyright: July 1, 2001

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 2 Issue 3

MLA
APA
Harvard
Chicago
Vancouver

MLA
APA
Harvard
Chicago
Vancouver

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

Copy

Copied to clipboard

BibTeX EndNote RIS

Published Online: 2001-07

You are currently not able to access this content.

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

Search journal Search the content of this journal

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

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