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6,XX Maleness and 46,XX 21-Hydroxylase Deficiency in Dizygotic Twins: Association or Coincidence?
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M.E. Atabek,
Veröffentlicht/Copyright:
1. Juni 2007
Published Online: 2007-06
©2011 by Walter de Gruyter GmbH & Co.
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Artikel in diesem Heft
- TABLE OF CONTENTS
- EDITORIAL
- An Update on the Treatment of Precocious Puberty in McCune-Albright Syndrome and Testotoxicosis
- European Society for Paediatric Endocrinology (ESPE)
- The Face of Late-onset Congenital Adrenal Hyperplasia
- Thyroid Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus: Prevalence and Risk Factors
- Neurocognitive Profile in Turner's syndrome is Not Affected by Growth Impairment
- Predicting the Growth Response to Growth Hormone (GH) Treatment in Prepubertal and Pubertal Children with Isolated GH Deficiency - Model Validation in an Observational Setting (GeNeSIS)
- The Course of Neonatal Cholestasis in Congenital Combined Pituitary Hormone Deficiency
- Criteria for Oral Glucose Tolerance Testing of Obese Minority Youth
- The Effects of Nutritional-Physical Activity School-based Intervention on Fatness and Fitness in Preschool Children
- Ghrelin - An Indicator for Fat Oxidation in Obese Children and Adolescents During a Weight Reduction Program
- Resolution of Severe Sinus Vein Thrombosis with Super Selective Thrombolysis in a Preadolescent with Diabetic Ketoacidosis and a Prothrombin Gene Mutation
- Remission of Congenital Diabetes Insipidus After Eight Years
- Metabolic Syndrome Manifestations in an Adolescent with Acrodysostosis
- 6,XX Maleness and 46,XX 21-Hydroxylase Deficiency in Dizygotic Twins: Association or Coincidence?
- CALENDAR
Artikel in diesem Heft
- TABLE OF CONTENTS
- EDITORIAL
- An Update on the Treatment of Precocious Puberty in McCune-Albright Syndrome and Testotoxicosis
- European Society for Paediatric Endocrinology (ESPE)
- The Face of Late-onset Congenital Adrenal Hyperplasia
- Thyroid Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus: Prevalence and Risk Factors
- Neurocognitive Profile in Turner's syndrome is Not Affected by Growth Impairment
- Predicting the Growth Response to Growth Hormone (GH) Treatment in Prepubertal and Pubertal Children with Isolated GH Deficiency - Model Validation in an Observational Setting (GeNeSIS)
- The Course of Neonatal Cholestasis in Congenital Combined Pituitary Hormone Deficiency
- Criteria for Oral Glucose Tolerance Testing of Obese Minority Youth
- The Effects of Nutritional-Physical Activity School-based Intervention on Fatness and Fitness in Preschool Children
- Ghrelin - An Indicator for Fat Oxidation in Obese Children and Adolescents During a Weight Reduction Program
- Resolution of Severe Sinus Vein Thrombosis with Super Selective Thrombolysis in a Preadolescent with Diabetic Ketoacidosis and a Prothrombin Gene Mutation
- Remission of Congenital Diabetes Insipidus After Eight Years
- Metabolic Syndrome Manifestations in an Adolescent with Acrodysostosis
- 6,XX Maleness and 46,XX 21-Hydroxylase Deficiency in Dizygotic Twins: Association or Coincidence?
- CALENDAR