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Clinical EEG and Neuroscience|November 29, 2012
Two siblings with similar phenotypes: one of them had ring 20 chromosomeF Irsel Tezer, Dilek Aktas, Mehmet Alikasifoglu, et al.
Intractable & Rare Diseases Research|March 31, 2017
Microdeletion of chromosome 1q21.3 in fraternal twins is associated with mental retardation, microcephaly, and epilepsyFatma Mujgan Sonmez, Eyyup Uctepe, Dilek Aktas, et al.
Medical Oncology (Northwood, London, England)|November 10, 2025
miR-770-5p: A novel molecular target regulating KLF4/EGFR signaling through PRMT5 interactionSenem Noyan, Bala Gur Dedeoglu, Alp Can, et al.
Psychiatry Investigation|August 3, 2016
Genetic Variations in Attention Deficit Hyperactivity Disorder Subtypes and Treatment Resistant CasesDilek Unal, Mehmet Fatih Unal, Mehmet Alikasifoglu, et al.
European Journal of Medical Genetics|February 14, 2006
Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogueG Eda Utine, Ayfer Alikasifoglu, Mehmet Alikasifoglu, et al.
Molecular Medicine Reports|August 12, 2016
A novel missense mutation of the GRK1 gene in Oguchi diseaseMehmet Yasin Teke, Mehmet Citirik, Serkan Kabacam, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 9, 2008
Factor V Leiden mutation and type 1 diabetes mellitusAsli Nar Demirer, Mehmet Alikasifoglu, Ergul Tuncbilek, et al.
European Journal of Medical Genetics|March 15, 2006
Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesisDilek Aktas, Mehmet Alikasifoglu, Nazli Gonc, et al.
Indian Journal of Pediatrics|September 2, 2008
Association of assisted reproductive technology with twinning and congenital anomaliesSevim Balci, Ozlem Engiz, Mehmet Alikasifoglu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 12, 2013
Methylene tetrahydrofolate reductase polymorphisms and homocysteine level in heart defectsUmit M Sahiner, Yasemin Alanay, Dursun Alehan, et al.
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