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Page 1
Sotos syndrome with septo-optic dysplasia.
Büyükgebiz A, Erçal D, Böber E. Büyükgebiz A, et al. Among authors: ercal d. J Pediatr Endocrinol Metab. 1996 Jul-Aug;9(4):497-9. doi: 10.1515/jpem.1996.9.4.497. J Pediatr Endocrinol Metab. 1996. PMID: 8910820
A toddler with a novel LEPR mutation.
Armağan C, Yılmaz C, Koç A, Abacı A, Ülgenalp A, Böber E, Erçal D, Demir K. Armağan C, et al. Among authors: ercal d. Hormones (Athens). 2019 Jun;18(2):237-240. doi: 10.1007/s42000-019-00097-6. Epub 2019 Feb 18. Hormones (Athens). 2019. PMID: 30778850
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
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.
49 results