A Second Locus (GLC3B) for Primary Congenital Glaucoma (Buphthalmos) Maps to the 1p36 Region von Akarsu, A. Nurten, Turacli, M. Erol, Aktan, S. Gulderen, Barsoum-Homsy, Magda, Chevrette, Line, Sayli, B. Sitki, Sarfarazi, Mansoor

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Assignment of a Locus (GLC3A) for Primary Congenital Glaucoma (Buphthalmos) to 2p21 and Evidence for Genetic Heterogeneity von Sarfarazi, Mansoor, Akarsu, Nurten A., Hossain, Altaf, Turacli, Erol M., Aktan, Gulderen S., Barsoum-Homsy, Magda, Chevrette, Line, Sayli, Sitki B.

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Arsenic-related Bowen's disease, palmar keratosis, and skin cancer von Cöl, M, Cöl, C, Soran, A, Sayli, B S, Oztürk, S

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Prenatal diagnosis of osteogenesis imperfecta type I by COL1A1 null-allele testing von Nuytinck, Lieve, Sayli, Bekir Sitki, Karen, Wettinck, De Paepe, Anne

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Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses von Wuyts, Wim, Van Hul, Wim, De Boulle, Kristel, Hendrickx, Jan, Bakker, Egbert, Vanhoenacker, Filip, Mollica, Florindo, Lüdecke, Hermann-Josef, Sayli, Bekir Sitki, Pazzaglia, Ugo E., Mortier, Geert, Hamel, Ben, Conrad, Ernest U., Matsushita, Mark, Raskind, Wendy H., Willems, Patrick J.

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Confined placental mosaicism in term placentae: Analysis of 125 cases von Artan, S., Başaran, N., Hassa, H., Özalp, S., Şener, T., Şayli, B. S., Cengiz, C., Özdemi̊, M., Durak, T., Dölen, I., Özgünen, T., Tuna, M.

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Genomic Structure of HOXD13 Gene: A Nine Polyalanine Duplication Causes Synpolydactyly in Two Unrelated Families von Akarsu, A. Nurten, Stoilov, Ivaylo, Yilmaz, Engin, Sayli, B. Sitki, Sarfarazi, Mansoor

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Boron concentrations in selected foods from borate-producing regions in Turkey von Simsek, Atilla, Velioglu, Y.Sedat, Coskun, A.Levent, Sayli, B.Sitki

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Ophthalmic Findings in GAPO Syndrome von I.lker, S.Sami, Öztürk, Faruk, Kurt, Emin, Temel, Mustafa, Gül, Davut, Saylı, Bekir Sıtkı

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Assessment of fertility and infertility in boron-exposed Turkish subpopulations: 3. Evaluation of fertility among sibs and in "borate families" von Sayli, B S

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Comparison of infertility rates in communities from boron-rich and boron-poor territories von Tüccar, E, Elhan, A. H, Yavuz, Y, Şayh, B. S

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A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data von Sayli, B S, Akarsu, A N, Sayli, U, Akhan, O, Ceylaner, S, Sarfarazi, M

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assessment of fertility in boron-exposed turkish subpopulations : 2. Evidence That Boron Has No Effect on Human Reproduction von Sayli, B S

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Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome von Sillén, Anna, Anton-Lamprecht, Ingrun, Braun-Quentin, Cordula, Kraus, Cornelia S., Sayli, Bekir Sitki, Ayuso, Carmen, Jagell, Sten, Küster, Wolfgang, Wadelius, Claes

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A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype? von Akarsu, A N, Akhan, O, Sayli, B S, Sayli, U, Baskaya, G, Sarfarazi, M

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Genetic features of retinitis pigmentosa in Turkey von ATMACA, L. S, SAYLI, B. S, AKARSU, N, GÜNDÜZ, K

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Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker von Sarfarazi, Mansoor, Akarsu, A.Nurten, Sayli, Bekir Sitki

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Bilateral split-hand with bilateral tibial aplasia von Sener, R N, Isikan, E, Diren, H B, Sayli, B S, Sener, F

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Tetra-oligodactyly with bilateral aplasia and hypoplasia of long bones of upper and lower limbs: a variable manifestation of the syndrome of ectrodactyly with tibial aplasia von Sener, R N, Sayli, B S, Isikan, U E, Ormeci, A R, Unsal, M, Tigdemir, M

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Antioxidative metabolism in Down syndrome von Tekşen, F, Sayli, B S, Aydin, A, Sayal, A, Işimer, A

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