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Molecular delineation of de novo small supernumerary marker chromosomes in prenatal diagnosis, a retrospective study |
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| Shuang Hu, Xiangdong Kong |
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Target enrichment long-read sequencing with adaptive sampling can determine the structure of the small supernumerary marker chromosomes |
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| Tasuku Mariya, Takema Kato, Takeshi Sugimoto, Syunsuke Miyai, Hidehito Inagaki, Tamae Ohye, Eiji Sugihara, Yukako Muramatsu, Seiji Mizuno, Hiroki Kurahashi |
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Prenatal diagnosis and genetic counseling of uniparental disomy |
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Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome |
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| Pascale Kleinfinger, Marie Brechard, Armelle Luscan, Detlef Trost, Aicha Boughalem, Mylene Valduga, Stéphane Serero DR, Jean-Marc Costa, Laurence Lohmann |
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| Yu-Min Syu, Juine-Yih Ma, Tzu-Hsuen Ou, Chung-Lin Lee, Hsiang-Yu Lin, Shuan-Pei Lin, Chia-Jung Lee, Chih-Ping Chen |
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| Igor N. Lebedev,Tatyana V. Karamysheva,Eugeny A. Elisaphenko,Alexey I. Makunin,Daria I. Zhigalina,Maria E. Lopatkina,Gleb V. Drozdov,Aleksander D. Cheremnykh,Natalia B. Torkhova,Gulnara N. Seitova,Stanislav A. Vasilyev,Anna A. Kashevarova,Ludmila P. Nazarenko,Nikolay B. Rubtsov |
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Whole Exome Sequencing Facilitated the Identification of a Mosaic Small Supernumerary Marker Chromosome (sSMC) |
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| Huan-xia Xing,Peng-bin Li,Li-min Cui,Jian-ye Jiang,Ning-ning Hu,Xiao-bin Zhang,Sercan Ergün |
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Molecular delineation of small supernumerary marker chromosomes using a single nucleotide polymorphism array |
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Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder |
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Genotype-phenotype correlation in 75 patients with small supernumerary marker chromosomes |
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| Tingting Li,Haiquan Sang,Guoming Chu,Yuanyuan Zhang,Manlong Qi,Xiaoliang Liu,Wanting Cui,Yanyan Zhao |
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A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature |
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| Veronica Bertini,Cecilia Giuliani,Maria Immacolata Ferreri,Alessandro Orsini,Alice Bonuccelli,Diego Peroni,Clara Bonaglia,Angelo Valetto |
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Molecular characterization of supernumerary marker chromosomes found as unexpected chromosome abnormalities in nine prenatal and nine postnatal samples |
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| Meena Lall, Anju Joshi, Shruti Agarwal, Preeti Paliwal, Pushpa Saviour, Surbhi Mahajan, Ratna Puri, Sunita Bijarnia, Ishwar Verma |
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Origin, Composition, and Structure of the Supernumerary B Chromosome of Drosophila melanogaster |
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| Stacey L. Hanlon,Danny E. Miller,Salam Eche,R. Scott Hawley |
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Complex Small Supernumerary Marker Chromosome Leading to Partial 4q/21q Duplications: Clinical Implication and Review of the Literature |
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| Fernanda T. Bellucco,Rodrigo A. Fock,Hélio R. de Oliveira-Júnior,Ana B. Perez,Maria I. Melaragno |
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Uniparental disomy and prenatal phenotype |
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| Xiaofei Li,Yan Liu,Song Yue,Li Wang,Tiejuan Zhang,Cuixia Guo,Wenjie Hu,Karl-Oliver Kagan,Qingqing Wu |
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Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization |
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| Mingran Sun,Han Zhang,Guiying Li,Carrie J. Guy,Xianfu Wang,Xianglan Lu,Fangchao Gong,Jiyun Lee,Susan Hassed,Shibo Li |
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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2 |
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| Chih-Ping Chen,Ming Chen,Shun-Ping Chang,Fang-Yu Hung,Meng-Ju Lee,Schu-Rern Chern,Peih-Shan Wu,Yen-Ni Chen,Shin-Wen Chen,Chen-Chi Lee,Dai-Dyi Town,Wen-Lin Chen,Wayseen Wang |
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| 25 |
Mosaic partial pericentromeric trisomy 8 and maternal uniparental disomy in a male patient with autism spectrum disorder |
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| Dina F. Ahram,Danae Stambouli,Aleksandra Syrogianni,Yasser Al-Sarraj,Spyridon Gerou,Hatem El-Shanti,Marios Kambouris |
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| Yu-an Hu,Yingxia Cui,Xiaobo Fan,Qiuyue WU,Weiwei Li,Weiping Wang |
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