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Fetal and Pediatric Pathology|November 19, 2019
Monitoring the Frequency and Duration of Hypoglycemia in Preterm Infants and Identifying Associated FactorsMaría Del Mar Fernández Martínez, José Luis Gómez Llorente, Jeronimo Momblan de Cabo, et al.
Fetal and Pediatric Pathology|November 19, 2019
Association of Neuregulin 1 rs7835688 G > C, rs16879552 T > C and rs2439302 G > C Polymorphisms with Susceptibility to Non-Syndromic Hirschsprung's DiseaseSeyed Hamed Hosseini-Jangjou, Seyed Alireza Dastgheib, Majid Aflatoonian, et al.
Fetal and Pediatric Pathology|November 19, 2019
Association of IL-6 -176G > C Polymorphism with Susceptibility to Preeclampsia: A Systematic Review and Meta-AnalysisMehrnaz Veisian, Atiyeh Javaheri, Nooshin Amjadi, et al.
Fetal and Pediatric Pathology|March 12, 2020
Pediatric Right Ventricular Cardiac Steatosis following Immunosuppressive TreatmentDiana Kozman, Carlos R Abramowsky, Janet Poulik, et al.
Fetal and Pediatric Pathology|March 7, 2020
Placental Expression of the Forelimb Patterning Transcription Factor MEIS2 in Trisomy 15Jennifer Pors, Tom Philipp, Jefferson Terry
Fetal and Pediatric Pathology|March 24, 2020
Clinical, biochemical and molecular spectrum of mild 6-pyruvoyl-tetrahydropterin synthase deficiency and a case reportBoyan Song, Zhijun Ma, Wei Liu, et al.
Fetal and Pediatric Pathology|March 12, 2020
Inner Ear Malformations in Congenital Deafness Are Not Associated with Increased Risk of Breech PresentationSlobodan Sekulic, Slobodanka Lemajic-Komazec, Ivana Sokolovac, et al.
Fetal and Pediatric Pathology|February 18, 2020
Antioxidant Activity and Oxidative Stress Status in Maternal Serum of β-thalassemic Mothers Carrying β-thalassemic Major and Normal FetusesYumna Fazal, Muhammad Zohaib, Zehra Hashim, et al.
Fetal and Pediatric Pathology|January 8, 2020
Association of BMP4 rs17563 Polymorphism with Nonsyndromic Cleft Lip with or without Cleft Palate Risk: Literature Review and Comprehensive Meta-AnalysisReza Bahrami, Seyed Alireza Dastgheib, Seyed Mohammadreza Niktabar, et al.
Fetal and Pediatric Pathology|January 31, 2020
Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing LossMahsa Farjami, Mozhgan Fathi, Mohammad Mehdi Ghasemi, et al.
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