Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
Alanay, Yasemin, Avaygan, Hrispima, Camacho, Natalia, Utine, G. Eda, Boduroglu, Koray, Aktas, Dilek, Alikasifoglu, Mehmet, Tuncbilek, Ergul, Orhan, Diclehan, Bakar, Filiz Tiker, Zabel, Bernard, Superti-Furga, Andrea, Bruckner-Tuderman, Leena, Curry, Cindy J.R., Pyott, Shawna, Byers, Peter H., Eyre, David R., Baldridge, Dustin, Lee, Brendan, Merrill, Amy E., Davis, Elaine C., Cohn, Daniel H., Akarsu, Nurten, Krakow, Deborah
Published in American journal of human genetics (09.04.2010)
Published in American journal of human genetics (09.04.2010)
Get full text
Journal Article
Methylene tetrahydrofolate reductase polymorphisms and homocysteine level in heart defects
Sahiner, Umit M, Alanay, Yasemin, Alehan, Dursun, Tuncbilek, Ergul, Alikasifoglu, Mehmet
Published in Pediatrics international (01.04.2014)
Published in Pediatrics international (01.04.2014)
Get full text
Journal Article
Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
Alanay, Yasemin, Avaygan, Hrispima, Camacho, Natalia, Utine, G. Eda, Boduroglu, Koray, Aktas, Dilek, Alikasifoglu, Mehmet, Tuncbilek, Ergul, Orhan, Diclehan, Bakar, Filiz Tiker, Zabel, Bernard, Superti-Furga, Andrea, Bruckner-Tuderman, Leena, Curry, Cindy J.R., Pyott, Shawna, Byers, Peter H., Eyre, David R., Baldridge, Dustin, Lee, Brendan, Merrill, Amy E., Davis, Elaine C., Cohn, Daniel H., Akarsu, Nurten, Krakow, Deborah
Published in American journal of human genetics (08.10.2010)
Published in American journal of human genetics (08.10.2010)
Get full text
Journal Article
CYP1A1 Gene Polymorphism and Risk of Epithelial Ovarian Neoplasm
Aktas, Dilek, Guney, Inci, Alikasifoglu, Mehmet, Yüce, Kunter, Tuncbilek, Ergul, Ayhan, Ali
Published in Gynecologic oncology (01.08.2002)
Published in Gynecologic oncology (01.08.2002)
Get full text
Journal Article
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair
Aktas, Dilek, Utine, Eda G, Mrasek, Kristin, Weise, Anja, von Eggeling, Ferdinand, Yalaz, Kalbiye, Posorski, Nicole, Akarsu, Nurten, Alikasifoglu, Mehmet, Liehr, Thomas, Tuncbilek, Ergul
Published in Molecular cytogenetics (28.05.2010)
Published in Molecular cytogenetics (28.05.2010)
Get full text
Journal Article
Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: importance of ACE polymorphism
Ozen, S, Alikasifoglu, M, Saatci, U, Bakkaloglu, A, Besbas, N, Kara, N, Kocak, H, Erbas, B, Unsal, I, Tuncbilek, E
Published in American journal of kidney diseases (01.07.1999)
Published in American journal of kidney diseases (01.07.1999)
Get more information
Journal Article
Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report
Aktas, Dilek, Weise, Anja, Utine, Eda, Alehan, Dursun, Mrasek, Kristin, von Eggeling, Ferdinand, Thieme, Heike, Tuncbilek, Ergul, Liehr, Thomas
Published in Molecular cytogenetics (30.06.2009)
Published in Molecular cytogenetics (30.06.2009)
Get full text
Journal Article
Gorlin Syndrome in Eleven Patients/On Bir Hastada Gorlin Sendromu
Utine, Gulen Eda, Alanay, Yasemin, Aktas, Dilek, Boduroglu, Koray, Alikasifoglu, Mehmet, Tuncbilek, Ergul
Published in The journal of pediatric research (01.06.2017)
Published in The journal of pediatric research (01.06.2017)
Get full text
Journal Article
Cavernous malformation with Poland-Möbius syndrome. Case illustration
Mut, Melike, Palaoglu, Selcuk, Alanay, Yasemin, Ismailoglu, Ozgur, Tuncbilek, Ergul
Published in Journal of neurosurgery (01.07.2007)
Published in Journal of neurosurgery (01.07.2007)
Get more information
Journal Article
CYP1A1 gene polymorphism and polycystic ovary syndrome
Esinler, Ibrahim, Aktas, Dilek, Otegen, Umit, Alikasifoglu, Mehmet, Yarali, Hakan, Tuncbileke, Ergul
Published in Reproductive biomedicine online (2008)
Published in Reproductive biomedicine online (2008)
Get full text
Journal Article
Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry
Utine, Gülen Eda, Şimşek-Kiper, Pelin Özlem, Akgün-Doğan, Özlem, Ürel-Demir, Gizem, Alanay, Yasemin, Aktaş, Dilek, Boduroğlu, Koray, Tunçbilek, Ergül, Alikaşifoğlu, Mehmet
Published in European journal of obstetrics & gynecology and reproductive biology (01.02.2018)
Published in European journal of obstetrics & gynecology and reproductive biology (01.02.2018)
Get full text
Journal Article
Gorlin Syndrome in Eleven Patients
Utine, Gülen Eda, Alanay, Yasemin, Aktaş, Dilek, Boduroğlu, Koray, Alikaşifoğlu, Mehmet, Tunçbilek, Ergül
Published in The journal of pediatric research (01.06.2017)
Published in The journal of pediatric research (01.06.2017)
Get full text
Journal Article
Factor V Leiden mutation and type 1 diabetes mellitus
Demirer, Asli Nar, Alikasifoglu, Mehmet, Tuncbilek, Ergul, Karakus, Sema, Erbas, Tomris
Published in Blood coagulation & fibrinolysis (01.01.2008)
Published in Blood coagulation & fibrinolysis (01.01.2008)
Get more information
Journal Article
Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH
Utine, Eda G, Alanay, Yasemin, Aktas, Dilek, Alikasifoglu, Mehmet, Boduroglu, Koray, Vermeesch, Joris, Tuncbilek, Ergul, Fryns, Jean-Pierre
Published in European journal of medical genetics (01.07.2008)
Published in European journal of medical genetics (01.07.2008)
Get full text
Journal Article
Cryptic trisomy 5q35.2qter and deletion lp36.3 characterised using FISH and array-based CGH
UTINE, Eda G, ALANAY, Yasemin, AKTAS, Dilek, ALIKASIFOGLU, Mehmet, BODUROGLU, Koray, VERMEESCH, Joris, TUNCBILEK, Ergul, FRYNS, Jean-Pierre
Published in European journal of medical genetics (2008)
Get full text
Published in European journal of medical genetics (2008)
Journal Article
Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis
Aktas, Dilek, Alikasifoglu, Mehmet, Gonc, Nazlı, Senocak, Mehmet E., Tuncbilek, Ergul
Published in European journal of medical genetics (01.03.2006)
Published in European journal of medical genetics (01.03.2006)
Get full text
Journal Article