Search Results - "BAHÇE, Muhterem"

Chromosome abnormalities in 1255 cleavage-stage human embryos by Márquez, Carmen, Sandalinas, Mireia, Bahçe, Muhterem, Al ikani, Mina, Munné, Santiago

“…The relationship was examined between chromosome abnormalities in cleavage stage human embryos and maternal age, embryo morphology and development rate…”
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Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia by Torun, Deniz, Nevruz, Oral, Akyol, Mesut, Kozan, Salih, Bahçe, Muhterem, Güran, Sefik, Beyan, Cengiz

“…Myeloproliferative neoplasms (MPNs) like essential thrombocythemia (ET), polycythemia vera (PV), and primary myelofibrosis (PMF) are acquired clonal…”
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Hyperhomocysteinemia and homozygous MTHFR 677C>T mutation finding in an Alzheimer's disease case with metabolic syndrome diagnosis by Guran, Sefik, Kozan, Salih, Bahçe, Muhterem

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Rare chromosomal complement of trisomy 21 in a boy conceived only by IVF by Guran, Sefik, Rosti, Rasim Ozgur, Sarıci, Serdar Ümit, Torun, Deniz, Kozan, Salih, Bahçe, Muhterem

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Methylation of SOCS3 in myeloproliferative neoplasms and secondary erythrocytosis/thrombocythemia / Miyeloproliferatif Neoplazmlar ve Sekonder Eritrositoz/Trombositemide SOCS3 Metilasyonu by Torun, Deniz, Nevruz, Oral, Akyol, Mesut, Kozanl, Salih, Bahce, Muhterem, Guran, Sefik, Beyan, Cengiz

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Preimplantation genetic diagnosis of aneuploidy: were we looking at the wrong chromosomes? by Bahçe, M, Cohen, J, Munné, S

“…Our purpose was to study aneuploidy frequencies of chromosomes 1, 4, 6, 7, 14, 15, 17, 18, and 22 in cleavage-stage embryos. These frequencies were compared to…”
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A case with oto-spondylo-mega-epiphyseal-dysplasia (OSMED): the clinical recognition and differential diagnosis by Karaer, Kadri, Rosti, Rasim Ozgür, Torun, Deniz, Sanal, Hatice Tuba, Bahçe, Muhterem, Güran, Sefik

“…The oto-spondylo-mega-epiphyseal-dysplasia (OSMED) phenotype is an autosomal recessive trait that is a skeletal dysplasia with the hallmark findings of limb…”
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Prenatal Diagnosis of Digeorge Syndrome by Ümit Göktolga, Kazım Gezginç, S. Temel Ceyhan, Ulaş Fidan, Ali Ergün, Muhterem Bahçe, iskender Başer

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Prenatal Diagnosis of Digeorge Syndrome by Göktolga, Ümit, Gezginç, Kazim, Ceyhan, S. Temel, Fidan, Ulaş, Ergün, Ali, Bahçe, Muhterem, Başer, Iskender

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Joubert syndrome with oculomotor apraxia: a case report by Rosti, Rasim Özgür; GATA Tıbbi Genetik BD, Kozan, Salih; GATA Tıbbi Genetik BD, Torun, Deniz; GATA Tıbbi Genetik BD, Bahçe, Muhterem; GATA Tıbbi Genetik BD, Güran, Şefik; GATA Tıbbi Biyoloji AD

“…In this paper,  a 7 month old male case born to a first degree cousin marriage, referred to our department for oculomotor apraxia and hypotonia, diagnosed as…”
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Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML by Akin, Dilara Fatma, Oner, Deniz Aslar, Mumcuoglu, Mine, Ezer, Ustun, Bahce, Muhterem, Kurekci, Emin, Akar, Nejat

“…Acute myeloid leukemia (AML) is a heterogeneous clonal disorder in terms of cytogenetic and molecular aberrations. Ten-Eleven-Translocation 2 (TET2), Kirsten…”
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A new approach to chromosomal abnormalities in sperm from patients with oligoasthenoteratozoospermia: detection of double aneuploidy in addition to single aneuploidy and diploidy by five-color fluorescence in situ hybridization using one probe set by Durakbasi-Dursun, Hatice Gul, Ph.D, Zamani, Ayse Gul, M.D.,Ph.D, Kutlu, Ruhusen, M.D, Görkemli, Hüseyin, M.D, Bahce, Muhterem, M.D.,Ph.D, Acar, Aynur, Ph.D

“…Objective To determine the frequencies of disomy, nullisomy, total aneuploidy, and diploidy in the sperms of infertile men. Design A controlled prospective…”
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Familial Hodgkin's Lymphoma from the Perspective of HLA by Sonmez, Mehmet, Erkut, Nergiz, Ucar, Fahri, Buruk, Kurtulus, Cobanoglu, Umit, Bahce, Muhterem, Ural, Ali Ugur

“…Although the incidence of Hodgkin lymphoma (HL) - a lymphoid tissue malignity - increases in the presence of several viruses, particularly EBV, as well as with…”
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The presence of MEFV gene mutations in patients with primary osteoarthritis who require surgery by Yilmaz, Sedat, Erdem, Hakan, Tunay, Servet, Torun, Deniz, Genc, Halil, Tunca, Yusuf, Karadag, Omer, Simsek, Ismail, Bahce, Muhterem, Pay, Salih, Dinc, Ayhan

“…Chronic arthritis of familial Mediterranean fever (FMF) involves weight-bearing joints and can occur in patients without a history of acute attack. Our aim was…”
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Differences in chromosome susceptibility to aneuploidy and survival to first trimester by Munné, Santiago, Bahçe, Muhterem, Sandalinas, Mireia, Escudero, Tomás, Márquez, Carmen, Velilla, Esther, Colls, Pere, Oter, Maria, Alikani, Mina, Cohen, Jacques

“…The purpose of this study was to find specific rates of aneuploidy in cleavage-stage embryos compared with first trimester data and to evaluate post-zygotic…”
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Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22 by Munné, Santiago, Magli, Cristina, Bahçe, Muhterem, Fung, Jingly, Legator, Mona, Morrison, Larry, Cohert, Jacques, Gianaroli, Luca

“…The present preimplantation diagnosis test is able to screen for the most common aneuploidies from single blastomeres in about five hours with a 15 per cent…”
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I(17q) in a case with myelodysplastic syndrome: an important and rarely seen chromosomal anomaly by Bahçe, Muhterem, Beyan, Cengiz, Erdem, Gökhan, Ateş, Ömer, Kozan, Salih, Torun, Deniz, Güran, Şefik

“…Myelodysplastic syndrome is a group of stem cell disorder that is characterized by ineffective hematopoiesis and transformation to acute leukemia. Genetic…”
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Coexistence of cytogenetic findings of trisomy 8, trisomy 9 and trisomy 21 in a case with acute myeloblastic leukemia by Kozan, Salih, Öztürk, Erman, Torun, Deniz, Bahçe, Muhterem, Kaya, Halide, Beyan, Cengiz, Güran, Şefik

“…The importance of genetic studies is great in the diagnosis and planning of the treatment of acute myeloblastic leukemia. Risk analysis should absolutely be…”
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The effect of cytogenetic analysis results on prognosis in cases with myelodysplastic syndrome by Güran, Şefik, Beyan, Cengiz, Tunca, Yusuf, Kozan, Salih, Torun, Deniz, Ifran, Ahmet, Kaptan, Kürşat, Ali Uğur Ural, Oral Nevruz, Avcu, Ferit, Türker Çetin, Gül, Davut, Bahçe, Muhterem

“…Cytogenetic analysis has a significant role in establishing diagnosis and prognostic evaluation of patients with myelodysplastic syndrome and is an important…”
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Spontaneous abortions are reduced after preconception diagnosis of translocations by Munné, S, Morrison, L, Fung, J, Márquez, C, Weier, U, Bahçe, M, Sable, D, Grundfeld, L, Schoolcraft, B, Scott, R, Cohen, J

“…Preimplantation genetic diagnosis of translocations has seldom been attempted. Recently, a genetic test based on analyzing polar bodies at the methaphase…”
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