Expressions of homeobox, collagen and estrogen genes in women with uterine prolapse von Dökmeci, Fulya, Tekşen, Fulya, Çetinkaya, Ş. Esra, Özkan, Tülin, Kaplan, Fuat, Köse, Kenan

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Genetic Screening Services Provided in Turkey von Erdem, Yurdagül, Tekşen, Fulya

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Apoptotic effects of salinomycin on human ovarian cancer cell line (OVCAR-3) von Kaplan, Fuat, Teksen, Fulya

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The Expression Levels of Klotho, Endothelial Nitrite Oxide Synthetase and Catalase Genes of the Heart Tissues of Young and Old Rats von Teksen, Fulya, Ozkan, Tulin, Hekmatshoar, Yalda, Turan, Belma

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Suggested components of the curriculum for nurses and midwives to enable them to develop essential knowledge and skills in genetics von Skirton, Heather, Barnoy, Sivia, Erdem, Yurdagul, Ingvoldstad, Charlotta, Pestoff, Rebecka, Teksen, Fulya, Williams, Jessica

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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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Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome von Frank, Valeska, Ortiz Brüchle, Nadina, Mager, Silke, Frints, Susanna G. M., Bohring, Axel, du Bois, Gabriele, Debatin, Irmgard, Seidel, Heide, Senderek, Jan, Besbas, Nesrin, Todt, Unda, Kubisch, Christian, Grimm, Tiemo, Teksen, Fulya, Balci, Sevim, Zerres, Klaus, Bergmann, Carsten

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Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome von Frank, Valeska, Ortiz Brüchle, Nadina, Mager, Silke, Frints, Susanna G. M., Bohring, Axel, du Bois, Gabriele, Debatin, Irmgard, Seidel, Heide, Senderek, Jan, Besbas, Nesrin, Todt, Unda, Kubisch, Christian, Grimm, Tiemo, Teksen, Fulya, Balci, Sevim, Zerres, Klaus, Bergmann, Carsten

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A true hermaphrodite case with 46, XY/46, XX karyotype von Tekyen, Feride Söylemez, Fulya

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Chorionic villus sampling (CVS) in cows von KAYMAZ, Mustafa, TEŞKEN, Fulya, ERTUĞRUL,Okan

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A 34-week-old male fetus with short rib polydactyly syndrome (SRPS) type I (Saldino-Noonan) with pancreatic cysts von Balci, Sevim, Altinok, Gülçin, Tekşen, Fulya, Eryilmaz, Muzaffer

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Prenatal diagnosis of Meckel-Gruber syndrome and Dandy-Walker malformation in four consecutive affected siblings, with the fourth one being diagnosed prenatally at 22 weeks of gest... von Balci, Sevim, Tekşen, Fulya, Dökmeci, Fulya, Cengiz, Bora, Cömert, Ruhi Bariş, Can, Bilge, Ozdamar, Sükrü

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