Publications
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | Second Faculty of Medicine
- Integrative role of the SALL4 gene: From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary2024 | Second Faculty of Medicine
- SALL4 phenotype in four generations of one family: An interplay of the upper limb, kidneys, and the pituitary2024 | Second Faculty of Medicine
- Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq2024 | Second Faculty of Medicine
- Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?2023 | Second Faculty of Medicine
- The invaluable role of consanguinity in providing insight into paediatric endocrine conditions: Lessons learned from congenital hyperinsulinism, monogenic diabetes, and short stature2022 | Second Faculty of Medicine
- Gregor Mendel and regulation of child's growth: genes, molecules, and paediatric clinical routine2022 | Second Faculty of Medicine
- Genetic etiology of small stature: news from the international conference ENDO Online 20212021 | Second Faculty of Medicine
- Congenital hyperinsulinism caused by novel homozygous katp channel gene variants may be linked to unexplained neonatal deaths among kurdish consanguineous families2020 | Second Faculty of Medicine
- Etiology and diagnostic approach of growth failure in children born small for gestational age (SGA) with persistent short stature in childhood (SGA-SS)2020 | Second Faculty of Medicine
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