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Two Cases With Neonatal Cholestasis and Renal Disorders Due to DCDC2 Mutation.
Teker Düztaş D, Sarı S, Eğritaş Gürkan Ö, Kayhan G, Dalgıç A, Dalgıç B. Teker Düztaş D, et al. Among authors: kayhan g. Exp Clin Transplant. 2022 May;20(Suppl 3):115-117. doi: 10.6002/ect.PediatricSymp2022.O37. Exp Clin Transplant. 2022. PMID: 35570614 Free article.
Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion.
Kayhan G, Calis P, Karcaaltincaba D, Tug E. Kayhan G, et al. J Obstet Gynaecol. 2019 Nov;39(8):1175-1176. doi: 10.1080/01443615.2019.1601165. Epub 2019 Jun 24. J Obstet Gynaecol. 2019. PMID: 31234679 Free article. No abstract available.
45 results