نتایج جستجو برای: symetric karyotype

تعداد نتایج: 9825  

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: : 2022

In this study, cytogenetic properties of A. escherichii were investigated using standard Giemsa staining, C-banding, and Ag-NOR staining techniques. The karyotype Sakarya bleak, the diploid chromosome number was 2n = 50, consists six pairs metacentric, 12 submetacentric, seven acrocentric autosomes (NF=86). No morphologically distinguishable heteromorphic sex chromosomes detected in karyotype. ...

Journal: :Vojnosanitetski Pregled 2023

Introduction. The presence of aneuploidy in patients diagnosed with chronic lymphocytic leukemia (CLL), except trisomy 12, is considered quite uncommon. Hyperdiploidy or near-tetraploidy (occurring 1?3% all CLL patients) usually confer a poor prognosis. Case report. We report patient progressive phase near?triploid karyotype. prognosis the disease was more precisely determined by applying cytog...

Journal: :Medical Entomology and Zoology 1995

2013
Byung Ho Choi Uk Hyun Kim Kun Soo Lee Cheol Woo Ko

PURPOSE 45,XY,t(13;14)(q10;q10) karyotype can suggest infertility associated with more or less severe oligospermia in male adults. In addition, 45,XX,t(13;14)(q10;q10) karyotype carries reproductive risks such as miscarriage or infertility in female adults. However, reports on the phenotype of this karyotype in children are very rare. This study was done to observe various phenotypes of this ka...

2015
Ediz Yeşilkaya Abdullah Bereket Feyza Darendeliler Firdevs Baş Şükran Poyrazoğlu Banu Küçükemre Aydın Şükran Darcan Bumin Dündar Muammer Büyükinan Cengiz Kara Erkan Sarı Erdal Adal Ayşehan Akıncı Mehmet Emre Atabek Fatma Demirel Nurullah Çelik Behzat Özkan Bayram Özhan Zerrin Orbak Betül Ersoy Murat Doğan Ali Ataş Serap Turan Damla Gökşen Ömer Tarım Bilgin Yüksel Oya Ercan Şükrü Hatun Enver Şimşek Ayşenur Ökten Ayhan Abacı Hakan Döneray Mehmet Nuri Özbek Mehmet Keskin Hasan Önal Nesibe Akyürek Kezban Bulan Derya Tepe Hamdi Cihan Emeksiz Korcan Demir Deniz Kızılay Ali Kemal Topaloğlu Erdal Eren Samim Özen Saygın Abalı Leyla Akın Beray Selver Eklioğlu Sultan Kaba Ahmet Anık Serpil Baş Tolga Ünüvar Halil Sağlam Semih Bolu Tolga Özgen Durmuş Doğan Esra Deniz Çakır Yaşar Şen Nesibe Andıran Filiz Çizmecioğlu Olcay Evliyaoğlu Gülay Karagüzel Özgür Pirgon Gönül Çatlı Hatice Dilek Can Fatih Gürbüz Çiğdem Binay Veysel Nijat Baş Kürşat Fidancı Adem Polat Davut Gül Cengizhan Açıkel Hüseyin Demirbilek Peyami Cinaz Carolyn Bondy

OBJECTIVE Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background of affected girls. This study aimed to systematically investigate the key clinical features of TS in relationship to karyotype in a large pediatric Turkish patient population. METHODS Our ...

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