Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome

I. Gennero,; T. Edouard,; Μ. Rashad,; Ε. Bieth,; F. Conte-Auriol,; F. Marin,; Μ. Tauber,; J.P. Salles,; Μ. El Kholy,

doi:10.1515/JPEM.2007.20.7.825

Startseite Medizin Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome

Artikel

Lizenziert

Nicht lizenziert Erfordert eine Authentifizierung

Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome

I. Gennero, , T. Edouard, , Μ. Rashad, , Ε. Bieth, , F. Conte-Auriol, , F. Marin, , Μ. Tauber, , J.P. Salles, und Μ. El Kholy,

Veröffentlicht/Copyright: 1. Juli 2007

Veröffentlicht von

Veröffentlichen auch Sie bei De Gruyter Brill

Manuskript einreichen Informationen für Autor*innen Erkunden Sie dieses Fachgebiet

Aus der Zeitschrift Journal of Pediatric Endocrinology and Metabolism Band 20 Heft 7

MLA
APA
Harvard
Chicago
Vancouver

MLA
APA
Harvard
Chicago
Vancouver

Gennero,, I., Edouard,, T., Rashad,, Μ., Bieth,, Ε., Conte-Auriol,, F., Marin,, F., Tauber,, Μ., Salles,, J.P. and El Kholy,, Μ.. "Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome" Journal of Pediatric Endocrinology and Metabolism, vol. 20, no. 7, pp. 825-832. https://doi.org/10.1515/JPEM.2007.20.7.825

Gennero,, I., Edouard,, T., Rashad,, Μ., Bieth,, Ε., Conte-Auriol,, F., Marin,, F., Tauber,, Μ., Salles,, J. & El Kholy,, Μ. (). Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome. Journal of Pediatric Endocrinology and Metabolism, 20(7), 825-832. https://doi.org/10.1515/JPEM.2007.20.7.825

Gennero,, I., Edouard,, T., Rashad,, Μ., Bieth,, Ε., Conte-Auriol,, F., Marin,, F., Tauber,, Μ., Salles,, J. and El Kholy,, Μ. () Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome. Journal of Pediatric Endocrinology and Metabolism, Vol. 20 (Issue 7), pp. 825-832. https://doi.org/10.1515/JPEM.2007.20.7.825

Gennero,, I., Edouard,, T., Rashad,, Μ., Bieth,, Ε., Conte-Auriol,, F., Marin,, F., Tauber,, Μ., Salles,, J.P. and El Kholy,, Μ.. "Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome" Journal of Pediatric Endocrinology and Metabolism 20, no. 7 (): 825-832. https://doi.org/10.1515/JPEM.2007.20.7.825

Gennero, I, Edouard, T, Rashad, Μ, Bieth, Ε, Conte-Auriol, F, Marin, F, Tauber, Μ, Salles, J, El Kholy, Μ. Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome. Journal of Pediatric Endocrinology and Metabolism. ;20(7): 825-832. https://doi.org/10.1515/JPEM.2007.20.7.825

Kopie

In die Zwischenablage kopiert

BibTeX EndNote RIS

Published Online: 2007-07

Sie haben derzeit keinen Zugang zu diesem Inhalt.

Artikel in diesem Heft

TABLE OF CONTENTS
EDITORIAL
Bariatric Surgery in Pediatrics - Is it Time?
LWPES 35 Years: Our Heritage and Our Destiny
Congenital Goiter in Premature Twins Due to Propylthiouracil Treatment
Low-Dose Adrenocorticotropic Hormone Stimulation Testing in Term Infants
Adrenal Function in Children with Severe Asthma Treated with High-Dose Inhaled Glucocorticoids: Recommended Screening Tests in Outpatient Conditions
Prevalence of Micropenis Among Boys from Different Regions of Bulgaria
C-Reactive Protein Levels and their Relationship with Metabolic Syndrome and Insulin Resistance in Mexican Adolescents
Usefulness of the Long-acting Insulin Analogue Glargine in Basal-Bolus Therapy for Japanese Children and Adolescents with Type 1 Diabetes Mellitus
Prevalence of Vitamin D Insufficiency in Obese Children and Adolescents
Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome
Infantile Systemic Hyalinosis with Early Thyroid Dysfunction
Can Insulinoma Cause Generalised Epilepsy?
Tumor Induced Hypercalcemia in a Patient with Mediastinal Synovial Sarcoma
ERRATUM. CALENDAR

Zeitschrift durchsuchen In dieser Zeitschrift suchen

https://doi.org/10.1515/JPEM.2007.20.7.825

Artikel in diesem Heft

TABLE OF CONTENTS
EDITORIAL
Bariatric Surgery in Pediatrics - Is it Time?
LWPES 35 Years: Our Heritage and Our Destiny
Congenital Goiter in Premature Twins Due to Propylthiouracil Treatment
Low-Dose Adrenocorticotropic Hormone Stimulation Testing in Term Infants
Adrenal Function in Children with Severe Asthma Treated with High-Dose Inhaled Glucocorticoids: Recommended Screening Tests in Outpatient Conditions
Prevalence of Micropenis Among Boys from Different Regions of Bulgaria
C-Reactive Protein Levels and their Relationship with Metabolic Syndrome and Insulin Resistance in Mexican Adolescents
Usefulness of the Long-acting Insulin Analogue Glargine in Basal-Bolus Therapy for Japanese Children and Adolescents with Type 1 Diabetes Mellitus
Prevalence of Vitamin D Insufficiency in Obese Children and Adolescents
Identification of a Novel Mutation in the Human Growth Hormone Receptor Gene (GHR) in a Patient with Laron Syndrome
Infantile Systemic Hyalinosis with Early Thyroid Dysfunction
Can Insulinoma Cause Generalised Epilepsy?
Tumor Induced Hypercalcemia in a Patient with Mediastinal Synovial Sarcoma
ERRATUM. CALENDAR