Challenges in child and adolescent health across the Arab Gulf countries—Focus on metabolic health حسب Basma Haris (12040355)

Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene حسب Basma Haris (12040355)

A Novel Homozygous <i>MC2R</i> Variant Leading to Type-1 Familial Glucocorticoid Deficiency حسب Idris Mohammed (751020)

مؤلفون آخرون: "…Basma Haris (12040355)…"

Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly حسب Umm-Kulthum Ismail Umlai (12040352)

مؤلفون آخرون: "…Basma Haris (12040355)…"

Infancy onset diabetes mellitus in a patient with a novel homozygous LRBA mutation حسب Iman Hawari (12561958)

مؤلفون آخرون: "…Basma Haris (12040355)…"

A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency حسب Sara Al-Khawaga (4792761)

مؤلفون آخرون:

The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar حسب Sara Al‐Khawaga (14778919)

مؤلفون آخرون:

Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient حسب Sanaa Sharari (12561952)

مؤلفون آخرون:

Understanding the Genetics of Early-Onset Obesity in a Cohort of Children From Qatar حسب Idris Mohammed (751020)

مؤلفون آخرون: "…Basma Haris (12040355)…"

Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi–Bickel Syndrome حسب Sanaa Sharari (12561952)

مؤلفون آخرون: