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Güncel Gönderiler: Tıbbi Biyoloji Anabilim Dalı

  • An Open Letter in Support of Transformative Biotechnology and Social Innovation: SANKO University Innovation Summit in Medicine and Integrative Biology, Gaziantep, Turkey, May 5-7, 2016. 
    Saygılı, Eyüp İlker; Abou-Zeid, Alaa H; Akkın, Salih Murat; Aklillu, Eleni; Barlas, İbrahim Ömer; Borda-Rodriguez, Alexander; Boschele, Filiz Aydoğan; Coşkun, Enes; Dağlı, Güner; Dai, Türkan Uğur; Eyigün, Can Polat; Georgakilas, Alexandros; Günbulut, Bircan; Güzelbey, Asım; Hekim, Can; Huzair, Farah; Kimyon, Sabit; Karakaş, Ümit; Masimirembwa, Collen; McNally, Ruth; Mete, Alper; Sancar, Peşvin; Steuten, Lotte M; Tanrıöver, Oylum; Tyfield, David; Töre, Volkan İhsan; Vuruşkan, Deniz; Wang, Wei; Yıldırım, Yusuf Ziya; Yılmaz, İsmet; Çetin, Zafer; Coşkun, Yavuz; Hekim, Nezih; Sınav, Ahmet; Dandara, Collet; Dereli, Türkay; Elbeyli, Levent; Endrenyi, Laszlo; Güngör, Kıvanç; Lin, Biaoyang; LLerena, Adrián; Srivastava, Sanjeeva; Warnich, Louise; Wonkam, Ambroise (MARY ANN LIEBERT, INC, 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA, 2016)
  • A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES 
    Çetin, Zafer; Clark, Ozden Altiok; Yakut, Sezin; Guzel, Nur Banu; Mihci, Ercan; Karauzum, Sibel Berker (2016)
    A molecularly characterized interstitial deletion encompassing the 11q14.1-q23.3 region in a case with multiple congenital abnormalities: Interstitial deletion of chromosome 11 long arm is a rare event. In most of the ...
  • Ultrasonographic and Cytogenetic Issues in Prenatal Diagnosis of Pallister Killian Syndrome. 
    Çetin, Zafer; Sanhal, Cem Yaşar; Karauzum, Sibel Berker; Mendilcioğlu, İbrahim İnanç; Yakut, Sezin (MEDECINE ET HYGIENE, CH DE LA MOUSSE 46, CASE POSTALE 475, CH-1225 CHENE-BOURG, SWITZERLAND, 2016)
  • The clinical spectrum of a rare chromosomal abnormality: Isochromosome 18p. 
    Nur, Banu Güzel; Clark, Ozden Altiok; Çetin, Zafer; Toylu, Aslı; Karauzum, Sibel Berker; Mihci, Ercan (MEDECINE ET HYGIENE, CH DE LA MOUSSE 46, CASE POSTALE 475, CH-1225 CHENE-BOURG, SWITZERLAND, 2016)
    Isochromosome 18p is a rare chromosomal disorder that occurs with a frequency of approximately one in every 180,000 live births, and affects both genders equally. MOst cases result from a de novo formation. In the ...
  • A familial interstitial 4q35 deletion with no discernible clinical effects. 
    Yakut, Sezin; Clark, Ozden Altiok; Sanhal, Cem Yaşar; Guzel, Nur Banu; Mendilcioğlu, İbrahim İnanç; Karaüzüm, Sibel Berker; Çetin, Zafer (WILEY-BLACKWELL, 111 RIVER ST, HOBOKEN 07030-5774, NJ USA, 2015)
    Small deletions on the long arm of distal chromosome 4 do not appear to result in gross congenital malformations, with the most frequently reported clinical findings including mild to moderate intellectual disability, ...
  • A PATIENT WITH AZOOSPERMIA AND 45,X/46,X,r(Y) (p11.2q11.2) MOSAICISM WITHOUT AZF DELETIONS. 
    Clark, Ozden Altiok; Koksal, Ismail Koksal; Karaüzüm, Sibel Berker; Çetin, Zafer (MEDECINE ET HYGIENE, CH DE LA MOUSSE 46, CASE POSTALE 475, CH-1225 CHENE-BOURG, SWITZERLAND, 2015)
  • PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH. 
    Yakut, Sezin; Çetin, Zafer; Sanhal, Cem Yaşar; Karaüzüm, Sibel Berker; Karaman, Birsen; Şimşek, Mehmet Masum (MEDECINE ET HYGIENE, CH DE LA MOUSSE 46, CASE POSTALE 475, CH-1225 CHENE-BOURG, SWITZERLAND, 2015)
    A 33 years-old pregnant woman was referred for amniocentesis at 19 weeks of gestation due to abnormal serum biochemistry. A non-satellited, monocentric marker chromosome was observed with a frequency of 50% in cultured ...
  • Chromosome abnormalities identified in 457 spontaneous abortions and their histopathological findings. 
    Yakut, Sezin; Toru, Havva Serap; Çetin, Zafer; Özel, Deniz; Şimşek, Mehmet; Mendilcioğlu, İnanç; Lüleci, Güven (2015)
    Objective: About 15% of clinically recognized pregnancies result in spontaneous abortion in the first trimester and the vast majority of these are the result of chromosome abnormalities. Studies of chromosomal constitutions ...
  • PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13). 
    Yakut, Sezin; Çetin, Zafer; Sanhal, Cem Yaşar; Karaman, Birsen; Mendilcioğlu, İbrahim İnanç; Karaüzüm, Sibel Berker (MEDECINE ET HYGIENE, CH DE LA MOUSSE 46, CASE POSTALE 475, CH-1225 CHENE-BOURG, SWITZERLAND, 2015)
    We here report a prenatal case with de novo pericentric inversion inv(2)(p11.2q13). A 20-years-old G1PO woman was referred for amniocentesis at 17 weeks of gestation, because of a positive second trimester screening test ...

Gazimuhtar Paşa Bulvarı
No:36
27090
Şehitkamil / GAZİANTEP