Search Results - "cytogenetics"

Clinical manifestations of chromosomal anomalies and polymorphic variations in patients suffering from reproductive failure by Leena Rawal, Sumit Kumar, Shiba Ranjan Mishra, Vandana Lal, Saurabh Kumar Bhattacharya

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A study on chromosomal analysis of patients with primary amenorrhea by Asoke K Pal, Prafulla S Ambulkar, Bharat R Sontakke, Shweta S Talhar, Pradeep Bokariya, Vijay K Gujar

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Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose? by Xiaoyi Cong, Tong Zhang, Zhenming Li, Xiaojin Luo, Liang Hu, Weiqiang Liu

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Sex assignment and psychosexual peculiarities of individuals with different forms of androgen insensitivity syndrome: A qualitative study by Jenaro Kristesashvili, Levan Kobaladze, Mariam Chipashvili, Anna Jibladze

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Predictive value of mid-trimester amniotic fluid high-sensitive C-reactive protein, ferritin, and lactate dehydrogenase for fetal growth restriction by Borna Sedigheh, Abdollahi Alireza, Mirzaei Fatemeh

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Daratumumab provides a survival benefit in relapsed and refractory Multiple Myeloma, independent of baseline clinical characteristics: A meta‐analysis by Congcong Cao, Xin Zhou, Qun Ma

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Influence of advanced age of maternal grandmothers on Down syndrome by Ramachandra Nallur B, Malini Suttur S

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Dysregulated angiogenesis in B-chronic lymphocytic leukemia: Morphologic, immunohistochemical, and flow cytometric evidence by Crawford Susan E, Goolsby Charles L, Kay Neil E, Frater John L, Dewald Gordon W, Peterson LoAnn C

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Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasound by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Comparison of 19-gauge conventional and Franseen needles for the diagnosis of lymphadenopathy and classification of malignant lymphoma using endoscopic ultrasound fine-needle aspir... by Mitsuru Okuno, Keisuke Iwata, Tsuyoshi Mukai, Yusuke Kito, Takuji Tanaka, Naoki Watanabe, Senji Kasahara, Yuhei Iwasa, Akihiko Sugiyama, Youichi Nishigaki, Yuhei Shibata, Junichi Kitagawa, Takuji Iwashita, Eiichi Tomita, Masahito Shimizu

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Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother by Chih-Ping Chen, Tsung-Hsien Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang

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Identification of heterochromatic variations in nonsyndromic cleft lip and palate by Soumya Raj, Leyon Varghese, Puthucode Viswanathan Narayanan, Suresh Kumar Raveendran, Pulikkottil Raphael Varghese, Alex George

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

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Multiple occurrence of psychomotor retardation and recurrent miscarriages in a family with a submicroscopic reciprocal translocation t(7;17)(p22;p13.2) by Magdalena Pasińska, Ewelina Łazarczyk, Katarzyna Jułga, Magdalena Bartnik-Głaska, Beata Nowakowska, Olga Haus

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Shwachman-Diamond syndrome: a complex case demonstrating the potential for misdiagnosis as asphyxiating thoracic dystrophy (Jeune syndrome) by Keogh Steven J, McKee Shane, Smithson Sarah F, Grier David, Steward Colin G

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Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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Podophyllum hexandrum ameliorates endosulfan-induced genotoxicity and mutagenicity in freshwater cyprinid fish crucian carp by Sabzar Ahmad Dar, Abdul Rehman Yousuf, Masood-, Bashir Ahmad Ganai, Mudasir Tantry, Farooz Ahmad Bhat

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A novel PAX5 rearrangement in TCF3-PBX1 acute lymphoblastic leukemia: a case report by Thayana Conceição Barbosa, Bruno Almeida Lopes, Caroline Barbieri Blunck, Marcela Braga Mansur, Adriana Vanessa Santini Deyl, Mariana Emerenciano, Maria S. Pombo-

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A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region by Tatyana A. Vasilyeva, Andrey V. Marakhonov, Marina E. Minzhenkova, Zhanna G. Markova, Nika V. Petrova, Natella V. Sukhanova, Philipp A. Koshkin, Denis V. Pyankov, Ilya V. Kanivets, Sergey A. Korostelev, Irina A. Krynskaya, Nadezhda V. Shilova, Sergey I. Kutsev, Vitaly V. Kadyshev, Rena A. Zinchenko

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Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang

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