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Journal of Pediatric Endocrinology & Metabolism : JPEM|July 12, 2018
Single center experience of biotinidase deficiency: 259 patients and six novel mutationsEbru Canda, Havva Yazici, Esra Er, et al.Clinical Dysmorphology|June 22, 2011
Homozygous mutation of CRLF-1 gene in a Turkish newborn with Crisponi syndromeHese Cosar, Zelal Kahramaner, Aydin Erdemir, et al.Journal of Tropical Pediatrics|December 27, 2023
SARS-CoV-2 reinfections in the pediatric cohort-a single-center experienceAsli Arslan, Zumrut Sahbudak Bal, Ece Erci, et al.Scandinavian Journal of Infectious Diseases|January 9, 2010
Interferon-gamma gene and interferon-gamma receptor-1 gene polymorphisms in children with tuberculosis from TurkeyHuseyin Onay, Aslihan Yilmaz Ekmekci, Burak Durmaz, et al.American Journal of Medical Genetics|November 20, 2002
Highest heterogeneity for cystic fibrosis: 36 mutations account for 75% of all CF chromosomes in Turkish patientsMehmet Okyay Kilinç, Vasiliki Ninidu Ninis, Elif Dağli, et al.Pediatric Pulmonology|October 1, 2015
MicroRNA expression profiling in children with different asthma phenotypesLevent Midyat, Figen Gulen, Emin Karaca, et al.Hemoglobin|June 16, 2015
Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion MutationFerda Ozkinay, Huseyin Onay, Emin Karaca, et al.Journal of Tropical Pediatrics|May 24, 2022
Clinical and Laboratory Findings of SARS-CoV-2 Infection in Children Younger than 6 Months Old: Neutropenia is More Common Not LymphopeniaGizem Guner Ozenen, Zumrut Sahbudak Bal, Nimet Melis Bilen, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|August 14, 2012
Association between bronchopulmonary dysplasia and MBL2 and IL1-RN polymorphismsBilin Cetinkaya Cakmak, Sebnem Calkavur, Ferda Ozkinay, et al.American Journal of Medical Genetics. Part A|December 1, 2020
A rare cause of syndromic short stature: 3M syndrome in three familiesEsra Isik, Duygu Arican, Tahir Atik, et al.Pageof 15