Askin Sen
Elazig, Turkey
Last Updated: 09/26/2026
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Found 8 publications
Clinical, biochemical and genotypical characteristics in biotinidase deficiency.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 04, 2021
Novel mutation in MASP1 gene in a new family with 3MC syndrome.
Journal: Clinical dysmorphology
Published: January 03, 2019
The Vitamin D Receptor Gene Polymorphisms in Asthmatic Children: A Case-Control Study.
Journal: Pediatric allergy, immunology, and pulmonology
Published: October 01, 2018
A rare mutation in the EPG5 gene causes Vici syndrome.
Journal: Clinical dysmorphology
Published: June 27, 2018
A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation.
Journal: Hormones (Athens, Greece)
Published: December 26, 2017
Mandibuloacral dysplasia and LMNA A529V mutation in Turkish patients with severe skeletal changes and absent breast development.
Journal: Clinical dysmorphology
Published: April 22, 2016
Chromosomal Translocation t (10;19) (q11.2;q13.4) in an Infertile Male.
Journal: The Eurasian journal of medicine
Published: April 24, 2013
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Last Updated: 09/26/2026