Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome

Publisher： Karger

E-ISSN： 1663-2826|88|2|119-126

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.88, Iss.2, 2017-07, pp. : 119-126

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Clinical, Endocrine, and Molecular Genetic Findings in Patients with 17β-Hydroxysteroid Dehydrogenase Deficiency

By  

Hormone Research in Paediatrics, Vol. 53, Iss. 1, 2000-08 ,pp. : 26-31

Karger

Access to resources Recommend Favorite

Clinical and Endocrine Features of Two Allan-Herndon-Dudley Syndrome Patients with Monocarboxylate Transporter 8 Mutations

By  

Hormone Research in Paediatrics, Vol. 83, Iss. 4, 2015-04 ,pp. : 288-292

Karger

Access to resources Recommend Favorite

Growth Hormone Insensitivity Syndrome (Laron Dwarfism)

By  

Hormone Research in Paediatrics, Vol. 49, Iss. 1, 2004-11 ,pp. : 47-48

Karger

Access to resources Recommend Favorite

Abnormal Growth in Noonan Syndrome: Genetic and Endocrine Features and Optimal Treatment

By  

Hormone Research in Paediatrics, Vol. 70, Iss. 3, 2008-07 ,pp. : 129-136

Karger

Access to resources Recommend Favorite

NREM Sleep Architecture and Relation to GH/IGF-1 Axis in Laron Syndrome

By  

Hormone Research in Paediatrics, Vol. 73, Iss. 5, 2010-04 ,pp. : 414-419

Karger

Access to resources Recommend Favorite