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Final Height in Patients with Constitutional Delay of Growth and Development from Tall Statured Families
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Otfrid Butenandt,
Published/Copyright:
February 1, 2005
Published Online: 2005-02
©2011 by Walter de Gruyter GmbH & Co.
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Articles in the same Issue
- TABLE OF CONTENTS
- The Management of Type 2 Diabetes Mellitus in Children and Adolescents
- 46,XX Patients with Congenital Adrenal Hyperplasia: Initial Assignment as Male, Reassigned Female
- Update on the Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency
- The Natural History and Genotype-Phenotype Nonconcordance of HLA Identical Siblings with the Same Mutations of the 21-Hydroxylase Gene
- Immunophenotypic Characterisation of Peripheral Blood Lymphocytes in Autoimmune Polyglandular Syndrome Type 1: Clinical Study and Review of the Literature
- Final Height in Patients with Constitutional Delay of Growth and Development from Tall Statured Families
- Constitutional Delay of Growth and Puberty: From Presentation to Final Height
- Longitudinal Investigation of the Relationship between Breast Milk Leptin Levels and Growth in Breast-fed Infants
- Leptin Profile in Neonatal Gonadotropin Surge and Relationship Between Leptin and Body Mass Index in Early Infancy
- Three New 46,XX Male Patients: A Clinical, Cytogenetic and Molecular Analysis
- Growth Hormone Deficiency in a Child with Williams-Beuren Syndrome. The Response to Growth Hormone Therapy
- Novel Growth Hormone Receptor Mutation in a Chinese Patient with Laron Syndrome
- Primary Hyperaldosteronism with Normokalaemia Secondary to an Adrenal Adenoma (Conn's Syndrome) in a 12 Year-old Boy
- Calendar
Articles in the same Issue
- TABLE OF CONTENTS
- The Management of Type 2 Diabetes Mellitus in Children and Adolescents
- 46,XX Patients with Congenital Adrenal Hyperplasia: Initial Assignment as Male, Reassigned Female
- Update on the Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency
- The Natural History and Genotype-Phenotype Nonconcordance of HLA Identical Siblings with the Same Mutations of the 21-Hydroxylase Gene
- Immunophenotypic Characterisation of Peripheral Blood Lymphocytes in Autoimmune Polyglandular Syndrome Type 1: Clinical Study and Review of the Literature
- Final Height in Patients with Constitutional Delay of Growth and Development from Tall Statured Families
- Constitutional Delay of Growth and Puberty: From Presentation to Final Height
- Longitudinal Investigation of the Relationship between Breast Milk Leptin Levels and Growth in Breast-fed Infants
- Leptin Profile in Neonatal Gonadotropin Surge and Relationship Between Leptin and Body Mass Index in Early Infancy
- Three New 46,XX Male Patients: A Clinical, Cytogenetic and Molecular Analysis
- Growth Hormone Deficiency in a Child with Williams-Beuren Syndrome. The Response to Growth Hormone Therapy
- Novel Growth Hormone Receptor Mutation in a Chinese Patient with Laron Syndrome
- Primary Hyperaldosteronism with Normokalaemia Secondary to an Adrenal Adenoma (Conn's Syndrome) in a 12 Year-old Boy
- Calendar