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Birth Defects Research|July 12, 2025
Microarray Application in Newborns With Multiple Congenital Anomalies: Genotype-Phenotype CorrelationRamazan Keçeci, Hayriye Nermin Keçeci, Müşerref Başdemirci
The Turkish Journal of Pediatrics|February 4, 2026
Hyperuricemia and elevated creatinine in a child with anemiaEmre Leventoğlu, Ayşe Şimşek, Hayriye Nermin Keçeci
Molecular Syndromology|May 13, 2026
Syndromic Alobar Holoprosencephaly Associated with a de novo 2p21p16.2 Contiguous Gene Deletion: A Neonatal Case ReportRamazan Keçeci, Hayriye Nermin Keçeci, Melek Büyükeren, et al.
Nephrology (Carlton, Vic.)|November 11, 2025
A TRIM8 Variant in a Child: Neuro-Renal Syndrome Causing Features Suggestive of Medullary Sponge KidneyEmre Leventoğlu, Hayriye Nermin Keçeci, Hatice Koçak Eker, et al.
The Turkish Journal of Pediatrics|July 24, 2026
A rare cause of congenital diarrhea: a homozygous AGR2 frameshift variant in an infantMelike Arslan, Hayriye Nermin Keçeci, Anna Carina Ergani, et al.
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