Approach to newborn priapism: A rare entity
Burgu, Berk, Talas, Halit, Erdeve, Omer, Karagol, Belma S, Fitoz, Suat, Soygur, Tarkan Y
Published in Journal of pediatric urology (01.12.2007)
Published in Journal of pediatric urology (01.12.2007)
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Supernumerary chromosome der(22)t(11;22): Emanuel syndrome associates with novel features
Yosunkaya Fenerci, E, Guven, G S, Kuru, D, Yilmaz, S, Tarkan-Argüden, Y, Cirakoglu, A, Deviren, A, Yüksel, A, Hacihanefioğlu, S
Published in Genetic counseling (01.01.2007)
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Published in Genetic counseling (01.01.2007)
Journal Article
Mosaic supernumerary r(8) syndrome
Yilmaz, S, Tarkan-Argüden, Y, Kuru, D, Deviren, A, Karaman, B, Yüksel, A, Hacihanefioğlu, S
Published in Genetic counseling (2005)
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Published in Genetic counseling (2005)
Journal Article
Cytogenetic Clonal Evolution in Patients with Chronic Myeloid Leukemia
Tarkan-Arguden, Y., Ar, M. Cem, Yilmaz, S., Ongoren, S., Kuru, D., Ure, U., Cırakoglu, A., Eskazan, A.E., Guven, G.S., Cetin, G., Purisa, S., Baslar, Z., Deviren, A., Aydin, Y., Hacıhanefioglu, S., Ferhanoglu, B., Tuzuner, N., Ulku, B., Soysal, T.
Published in Biotechnology, biotechnological equipment (01.01.2009)
Published in Biotechnology, biotechnological equipment (01.01.2009)
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A small supernumerary marker chromosome X identified by in situ hybridization
Silahtaroglu, A N, Hacihanefioglu, S, Yilmaz, S, Tarkan, Y, Cenani, A, Tümer, Z
Published in Clinical genetics (01.05.1995)
Published in Clinical genetics (01.05.1995)
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Journal Article
De Novo X/X Translocation in a Patient with Secondary Amenorrhea
Tarkan, Yelda, Hacihanefioǧlu, Seniha, Silahtaroǧlu, Asli N., Deviren, Ayhan, Topçuoǧlu, Deniz, Cenani, Asim
Published in Hereditas (01.01.1995)
Published in Hereditas (01.01.1995)
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