Arama Sonuçları - "fluorescence in situ hybridization"

Epithelioid cell histiocytoma with SQSTM1-ALK fusion: a case report Yazar: Ryuko Nakayama, Yuki Togashi, Satoko Baba, Yo Kaku, Yuki Teramoto, Takaki Sakurai, Hironori Haga, Kengo Takeuchi

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Rapid progression of a low-grade follicular lymphoma with foci of high proliferation index and BCL6 rearrangement into a diffuse large B-cell lymphoma: A case report and review of... Yazar: Simran Kalsi, BS, Steven Gersen, PhD, Ronald Harris, DO, Jagmohan S. Sidhu, MD

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Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis Yazar: Francesco Libotte, Domenico Bizzoco, Ivan Gabrielli, Alvaro Mesoraca, Pietro Cignini, Salvatore Giovanni Vitale, Ilaria Marilli, Ferdinando Antonio Gulino, Agnese Maria Chiara Rapisarda, Claudio Giorlandino

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral rad... Yazar: Chih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen, Fang-Tzu Wu, Schu-Rern Chern, Peih-Shan Wu, Yun-Yi Chen, Wen-Lin Chen, Wayseen Wang

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Chromosome (re)positioning in spermatozoa of fathers and sons - carriers of reciprocal chromosome translocation (RCT) Yazar: Marta Olszewska, Ewa Wiland, Nataliya Huleyuk, Monika Fraczek, Alina T. Midro, Danuta Zastavna, Maciej Kurpisz

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Comparison of chromosomal instability of human amniocytes in primary and long-term cultures in AmnioMAX II and DMEM media: A cross-sectional study Yazar: Seyed Mehdi Hoseini, Fateme Montazeri, Maryam Moghaddam-Matin, Ahmad Reza Bahrami, Hassan Heidarian Meimandi, Saeed Ghasemi-Esmailabad, Seyed Mehdi Kalantar

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Sarcomatoid malignant peritoneal mesothelioma: A rare case of sarcomatoid component with monosomy 9 appeared in ascites fluid Yazar: Yuri Noda, Yuko Nakanishi, Kumi Masuda, Masaru Yamasaki

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Chromosome microarray analysis combined with karyotype analysis is a powerful tool for the detection in pregnant women with high-risk indicators Yazar: Guanhua Qian, Liuyun Cai, Hong Yao, Xiaojing Dong

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Prognostic role of ALK-1 and h-TERT expression in glioblastoma multiforme: correlation with ALK gene alterations Yazar: Dalia Elsers, Doaa F. Temerik, Alia M. Attia, A. Hadia, Marwa T. Hussien

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Prenatal diagnosis of mosaic tetrasomy 18p Yazar: Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Dai-Dyi Town, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome Yazar: Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang

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Low-grade papillary Schneiderian carcinoma with TP53 mutation: a case report and review of the literature Yazar: Sayaka Yuzawa, Tomohiko Michizuka, Rika Kakisaka, Yusuke Ono, Manami Hayashi, Miki Takahara, Akihiro Katada, Yusuke Mizukami, Mishie Tanino

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GH successful treatment in a female with a de novo 46,XX,add(X)(p36),t(X;Y)(p36.3;p11.2), growth impairment and SHOX-haploinsufficiency Yazar: Maria Cristina Maggio, Giovanni Corsello

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Primary intra-axial Ewing sarcoma of the central nervous system: report of a rare case with literature review Yazar: Fikret Dirilenoğlu, Mthabisi Talent George Moyo, Aslı Kahraman

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Pontiac fever: an operational definition for epidemiological studies Yazar: Mathieu Laurence, Hartemann Philippe, Zmirou-Navier Denis, Deloge-Abarkan Magali, Tossa Paul

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Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome Yazar: Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Yu-Peng Liu, Yu-Ling Kuo, Yen-Ni Chen, Peih-Shan Wu, Dai-Dyi Town, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

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Chromosomal causes of hypergonadotropic hypogonadism in women and men. Literature review Yazar: О. А. Бурка, Л. П. Кузьмук, Г.О. Ісламова, С. В. Овчаренко

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Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallo... Yazar: Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

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Glial- and Neuronal-Specific Expression of CCL5 mRNA in the Rat Brain Yazar: Maria Fe Lanfranco, Maria Fe Lanfranco, Italo Mocchetti, Italo Mocchetti, Mark P. Burns, Sonia Villapol

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Evaluation of 7q31 region improves the accuracy of <it>EGFR </it>FISH assay in non small cell lung cancer Yazar: Venesio Tiziana, Ferrero Paolo, Corigliano Mara, Casorzo Laura, Risio Mauro

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