Risultati della ricerca - Li, Peining

Fluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research Applications di Cui, Chenghua, Shu, Wei, Li, Peining

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Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies di Hu, Qiping, Chai, Hongyan, Shu, Wei, Li, Peining

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Absence of aneuploidy and gastrointestinal tumours in a man with a chromosomal 2q13 deletion and BUB1 monoallelic deficiency di Hoang, Don, Sue, Gloria R, Xu, Fang, Li, Peining, Narayan, Deepak

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Prenatal Diagnosis and Postnatal Followup of Partial Trisomy 13q and Partial Monosomy 10p: A Case Report and Review of the Literature di Wei, Yuan, Gao, Xuefeng, Yan, Liying, Xu, Fang, Li, Peining, Zhao, Yangyu

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Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities di Xu, Zhiyong, Geng, Qian, Luo, Fuwei, Xu, Fang, Li, Peining, Xie, Jiansheng

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De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome di Wang, Qin, Geng, Qian, Zhou, Qinghua, Luo, Fuwei, Li, Peining, Xie, Jiansheng

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The impact of novel coronavirus SARS-CoV-2 among healthcare workers in hospitals: An aerial overview di Xiang, Boqi, Li, Peining, Yang, Xinhui, Zhong, Shuyi, Manyande, Anne, Feng, Maohui

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Inverted duplication, triplication and quintuplication through sequential breakage‐fusion‐bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion di Chai, Hongyan, Grommisch, Brittany, DiAdamo, Autumn, Wen, Jiadi, Hui, Pei, Li, Peining

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Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma di Chai, Hongyan, Xu, Fang, DiAdamo, Autumn, Grommisch, Brittany, Mao, Huanzhi, Li, Peining

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Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin di Zerjav, Marie, DiAdamo, Autumn, Grommisch, Brittany, Katherine, Amato, Chai, Hongyan, Peng, Gang, Li, Peining

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Genotype–Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature di Xie, Xiaolei, Chai, Hongyan, DiAdamo, Autumn, Grommisch, Brittany, Wen, Jiadi, Zhang, Hui, Li, Peining

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Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability di Xu, Fang, Li, Lun, Schulz, Vincent P, Gallagher, Patrick G, Xiang, Bixia, Zhao, Hongyu, Li, Peining

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FISH panel for leukemic CTCL di Weed, Jason, Gibson, Juliet, Lewis, Julia, Carlson, Kacie, Foss, Francine, Choi, Jaehyuk, Li, Peining, Girardi, Michael

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Correlating genomic copy number alterations with clinicopathologic findings in 75 cases of hepatocellular carcinoma di Peng, Gang, Chai, Hongyan, Ji, Weizhen, Lu, Yufei, Wu, Shengming, Zhao, Hongyu, Li, Peining, Hu, Qiping

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A Highly Sensitive, High-Throughput Assay for the Detection of Turner Syndrome di Rivkees, Scott A., Hager, Karl, Hosono, Seiyu, Wise, Anastasia, Li, Peining, Rinder, Henry M., Gruen, Jeffrey R.

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Changes in and Efficacies of Indications for Invasive Prenatal Diagnosis of Cytogenomic Abnormalities: 13 Years of Experience in a Single Center di Meng, Jinlai, Matarese, Chelsea, Crivello, Julianna, Wilcox, Katherine, Wang, Dongmei, DiAdamo, Autumn, Xu, Fang, Li, Peining

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Bi-allelic Deletions within 13q14 and Transient Trisomy 21 with absence of GATA1s in Pediatric Acute Megakaryoblastic Leukemia di Massaro, Stephanie A., Bajaj, Renu, Pashankar, Farzana D., Ornstein, Deborah, Gallagher, Patrick G., Krause, Diane S., Li, Peining

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Xp22.2 Chromosomal Duplication in Familial Intracranial Arachnoid Cyst di Furey, Charuta G., Timberlake, Andrew T., Nelson-Williams, Carol, Duran, Daniel, Li, Peining, Jackson, Eric M., Kahle, Kristopher T.

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Integrated FISH, Karyotyping and aCGH Analyses for Effective Prenatal Diagnosis of Common Aneuploidies and Other Cytogenomic Abnormalities di Chai, Hongyan, DiAdamo, Autumn, Grommisch, Brittany, Boyle, Jennifer, Amato, Katherine, Wang, Dongmei, Wen, Jiadi, Li, Peining

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Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus di Bogardus, Hannah, Schulz, Vincent P., Maksimova, Yelena, Miller, Barbara A., Li, Peining, Forget, Bernard G., Gallagher, Patrick G.

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