Search Results - "cytogenetics"

Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocation by Judith Fan, T. Niroshini Senaratne, Jason Y. Liu, Michelle Bina, Julian A. Martinez-Agosto, Fabiola Quintero-Rivera, Jessica J. Wang

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Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses by Chih-Ping Chen, Hsien-Ming Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang

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Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang

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Preclinical Evaluation of the Tumorigenic and Immunomodulatory Properties of Human Bone Marrow Mesenchymal Stromal Cell Populations with Clonal Trisomy 5 by Maria Susana Joya Marodin, Juliana A. Godoy, Raquel M. Alves-Paiva, Kelen Alvarez, Thiago Giove Mitsugi, Ana Cristina Victorino Krepischi, Nelson Hamerschlak, Maria Augusta Tezelli Bortolini, Rodrigo Castro, Andrea T. Kondo, Jose Mauro Kutner, Oswaldo Keith Okamoto

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Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia by Chih-Ping Chen, Yi-Ning Su, Ming-Huei Lin, Tao-Yeuan Wang, Schu-Rern Chern, Yu-Ling Kuo, Yu-Ting Chen, Wayseen Wang

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The spectrum of chromosomal abnormalities and endocrine profile of male infertility with nonobstructive semen abnormality: A case-control study by Paresh Singhal, Ganesh Pendkur, Rituraj Singh Parihar, Sharanjit Singh, Barun Kumar Chakrabarty, S K Raghavendra

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Challenges of Turner Syndrome Care in Adulthood: A Single Tertiary Center Experience by Ralitsa Robeva, Atanaska Elenkova, Sabina Zacharieva

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Recurrent pregnancy loss: current perspectives by El Hachem H, Crepaux V, May-Panloup P, Descamps P, Legendre G, Bouet PE

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Osteogenesis imperfecta type IV: Prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Ming-Huei Lin, Jun-Wei Su, Wayseen Wang

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Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound by Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang, Chen-Chi Lee

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Characterization of Immunophenotypic Aberrancies in Adult and Childhood Acute Lymphoblastic Leukemia: Lessons from Regional Variation by Mitra Rezaei, Sandra Refoua, Najme Esfandiari, Masoud Shamaei

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Lipoma y Lipomatosis Lipoma and Lipomatosis by L Huczak, N E Driban

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Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case rep... by Ruen Yao, Tingting Yu, Yufei Xu, Guoqiang Li, Lei Yin, Yunfang Zhou, Jian Wang, Zhilong Yan

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Genetic investigations on 8 patients affected by ring 20 chromosome syndrome by Giordano Lucio, Accorsi Patrizia, Finelli Palma, Marchi Margherita, Camporeale Nicole, Russo Silvia, Recalcati Maria, Ballarati Lucia, Vignoli Aglaia, Giardino Daniela, La Briola Francesca, Chiesa Valentina, Canevini Maria, Larizza Lidia

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Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Shin-Yu Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang

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Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy by Chih-Ping Chen, Schu-Rern Chern, Liang-Kai Wang, Peih-Shan Wu, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang

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Detection rates of abnormalities in over 10,000 amniotic fluid samples at a single laboratory by Sha Lu, Nisile Kakongoma, Wen-sheng Hu, Yan-zhen Zhang, Nan-nan Yang, Wen Zhang, Ai-fen Mao, Yi Liang, Zhi-fen Zhang

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Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amnioc... by Chih-Ping Chen, Shing-Jyh Chang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang

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Variații cromozomiale la bărbații infertili. by Stela Racoviță, Svetlana Capcelea, Veaceslav Moşin, Elena Halabudenco, Ana Mişina, Tatiana Samoilenco, Svetlana Hadjiu, Mariana Sprincean

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Outcome and factors affecting survival of childhood myelodysplastic syndrome; single centre experience by Amr Abdalla, Mahmoud Hammad, Hanafy Hafez, Sherine Salem, Sonya Soliman, Salma Ghazal, Omayma Hassanain, Alaa El-Haddad

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