Authors: Percin, EF Guvenal, T Cetin, A Percin, S Goze, F Arici, S

Citation: Ef. Percin et al., First-trimester diagnosis of Robinow syndrome, FETAL DIAGN, 16(5), 2001, pp. 308-311

Authors: Percin, EF Ploder, LA Yu, JJ Arici, K Horsford, DJ Rutherford, A Bapat, B Cox, DW Duncan, AMV Kalnins, VI Kocak-Altintas, A Sowden, JC Traboulsi, E Sarfarazi, M McInnes, RR

Citation: Ef. Percin et al., Human microphthalmia associated with mutations in the retinal homeobox gene CHX10, NAT GENET, 25(4), 2000, pp. 397-401

Authors: van Bokhoven, H Celli, J Kayserili, H van Beusekom, E Balci, S Brussel, W Skovby, F Kerr, B Percin, EF Akarsu, N Brunner, HG

Citation: H. Van Bokhoven et al., Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome, NAT GENET, 25(4), 2000, pp. 423-426

Authors: Percin, EF Bulut, S Kunt, T Percin, S Bulut, O Sungu, S

Citation: Ef. Percin et al., Waardenburg syndrome type I and small patella syndrome in the same patient, PEDIATR INT, 41(6), 1999, pp. 704-706

Authors: Koyluoglu, G Percin, EF

Citation: G. Koyluoglu et Ef. Percin, An infant with situs inversus totalis, branchial cleft cyst and ectopic kidney: a new combination?, CLIN DYSMOR, 8(3), 1999, pp. 233-234

Authors: Percin, EF Percin, S

Citation: Ef. Percin et S. Percin, A new combination: short stature, congenital unilateral absence of the fibula, oligodactyly and trigonocephaly, CLIN DYSMOR, 8(1), 1999, pp. 67-68