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Page 1
Congenital chylothorax.
Ozkan H, Ay N, Ozaksoy D, Ercal D, Erata Y, Durak H, Evyapan O, Toprak S. Ozkan H, et al. Among authors: ercal d. Turk J Pediatr. 1996 Jan-Mar;38(1):113-7. Turk J Pediatr. 1996. PMID: 8819631
Goldston syndrome: report of a case.
Gulcan YH, Duman N, Kumral A, Sağol, Lebe B, Kavukçu S, Erçal D, Celiloğlu M, Ozkan H. Gulcan YH, et al. Among authors: ercal d. Genet Couns. 2001;12(3):263-7. Genet Couns. 2001. PMID: 11693790
Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum.
Çakmaklı S, Çankaya T, Gürsoy S, Koç A, Kırbıyık Ö, Kılıçarslan ÖA, Özer E, Erçal D, Bozkaya ÖG. Çakmaklı S, et al. Among authors: ercal d. Cytogenet Genome Res. 2017;153(4):175-180. doi: 10.1159/000486775. Epub 2018 Mar 9. Cytogenet Genome Res. 2017. PMID: 29518772 Review.
Lymphoid tissue histology in a patient with ICF syndrome.
Makay B, Anal O, Köse G, Bozkaya O, Ozer E, Bora E, Ulgenalp A, Erçal D. Makay B, et al. Among authors: ercal d. J Investig Allergol Clin Immunol. 2012;22(3):220-1. J Investig Allergol Clin Immunol. 2012. PMID: 22697015 Free article. No abstract available.
Tricho-rhino-phalangeal syndrome type I.
Eroğlu Y, Erçal D. Eroğlu Y, et al. Among authors: ercal d. Turk J Pediatr. 1996 Oct-Dec;38(4):537-42. Turk J Pediatr. 1996. PMID: 8993187
Congenital cardiac defects with 22q11 deletion.
Giray O, Ulgenalp A, Bora E, Sağin Saylam G, Unal N, Meşe T, Hüdaoğlu S, Erçal D. Giray O, et al. Among authors: ercal d. Turk J Pediatr. 2003 Jul-Sep;45(3):217-20. Turk J Pediatr. 2003. PMID: 14696799
49 results