Use of whole exome sequencing for identification of genetic variants related to Growth Hormone Deficiency and Short Stature: A Family-Based Study.

Alharazy, Shatha; Naseer, Muhammad Imran

Alharazy, Shatha; Naseer, Muhammad Imran.

Afiliación

Alharazy S; Shatha Alharazy Department of Physiology, Faculty of Medicine, Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Naseer MI; Muhammad Imran Naseer Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

Pak J Med Sci ; 39(5): 1337-1344, 2023.

Article en En | MEDLINE | ID: mdl-37680843

Palabras clave

Growth hormone deficiency; Polymorphisms; Short stature; Vitamin-D; Vitamin-D deficiency; Whole exome sequencing

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Pak J Med Sci Año: 2023 Tipo del documento: Article País de afiliación: Arabia Saudita Pais de publicación: Pakistán

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