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45,X/46,XX mosaicism in patients with idiopathic premature ovarian failure
Devi, Anne S., Metzger, Deborah A., Luciano, Anthony A., Benn, Peter A.
Published in Fertility and sterility (01.07.1998)
Published in Fertility and sterility (01.07.1998)
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An epidemiological and aetiological study of children with intellectual disability in Taiwan
Hou, J.-W., Wang, T.-R., Chuang, S.-M.
Published in Journal of intellectual disability research (01.04.1998)
Published in Journal of intellectual disability research (01.04.1998)
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Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study
Zhuang, Jianlong, Zhang, Na, Chen, Yu’e, Jiang, Yuying, Chen, Xinying, Chen, Wenli, Chen, Chunnuan
Published in Scientific reports (27.01.2024)
Published in Scientific reports (27.01.2024)
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Molecular cytogenetic characterization of isolated recurrent 4q35.2 microduplication in Chinese population: a seven-year single-center retrospective study
Zhuang, Jianlong, Wei, Qiulan, Jiang, Yuying, Zeng, Shuhong, Lou, Haijuan, Zhang, Na, Chen, Chunnuan
Published in BMC pregnancy and childbirth (18.09.2024)
Published in BMC pregnancy and childbirth (18.09.2024)
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Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
Rajcan-Separovic, E, Harvard, C, Liu, X, McGillivray, B, Hall, J G, Qiao, Y, Hurlburt, J, Hildebrand, J, Mickelson, E C R, Holden, J J A, Lewis, M E S
Published in Journal of medical genetics (01.04.2007)
Published in Journal of medical genetics (01.04.2007)
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Molecular cytogenetic analysis reveals the existence of two independent neo-XY sex chromosome systems in Anatolian Pamphagidae grasshoppers
Jetybayev, Ilyas Yerkinovich, Bugrov, Alexander Gennadievich, Ünal, Mustafa, Buleu, Olesya Georgievna, Rubtsov, Nikolay Borisovich
Published in BMC evolutionary biology (07.02.2017)
Published in BMC evolutionary biology (07.02.2017)
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Neuroendocrine Tumors of the Prostate: Emerging Insights from Molecular Data and Updates to the 2016 World Health Organization Classification
Priemer, David S., Montironi, Rodolfo, Wang, Lisha, Williamson, Sean R., Lopez-Beltran, Antonio, Cheng, Liang
Published in Endocrine pathology (01.06.2016)
Published in Endocrine pathology (01.06.2016)
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Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3
Vetro, Annalisa, Dehghani, Mohammad Reza, Kraoua, Lilia, Giorda, Roberto, Beri, Silvana, Cardarelli, Laura, Merico, Maurizio, Manolakos, Emmanouil, Parada-Bustamante, Alexis, Castro, Andrea, Radi, Orietta, Camerino, Giovanna, Brusco, Alfredo, Sabaghian, Marjan, Sofocleous, Crystalena, Forzano, Francesca, Palumbo, Pietro, Palumbo, Orazio, Calvano, Savino, Zelante, Leopoldo, Grammatico, Paola, Giglio, Sabrina, Basly, Mohamed, Chaabouni, Myriam, Carella, Massimo, Russo, Gianni, Bonaglia, Maria Clara, Zuffardi, Orsetta
Published in European journal of human genetics : EJHG (01.08.2015)
Published in European journal of human genetics : EJHG (01.08.2015)
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Prenatal diagnosis and molecular cytogenetic analysis of a de novo isodicentric chromosome 18
Zhang, Yanliang, Dai, Yong, Ren, Jinghui, Wang, Linqian
Published in Annals of Saudi medicine (01.11.2010)
Published in Annals of Saudi medicine (01.11.2010)
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Molecular cytogenetic analysis of head and neck squamous cell carcinoma: By comparative genomic hybridization, spectral karyotyping, and expression array analysis
Squire, Jeremy A., Bayani, Jane, Luk, Catherine, Unwin, Lianne, Tokunaga, Jason, MacMillan, Christina, Irish, Jonathan, Brown, Dale, Gullane, Patrick, Kamel-Reid, Suzanne
Published in Head & neck (01.09.2002)
Published in Head & neck (01.09.2002)
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Infant Acute Lymphoblastic Leukemias Are Pan-Sensitive to Obatoclax Across molecular/Cytogenetic Subtypes, Especially MLL-ENL, and gene Expression Profiles Determine Obatoclax IC50: A Report on the Children's Oncology Group (COG) P9407 Trial
Urtishak, Karen A., Wang, Li-San, Harvey, Richard, Atlas, Susan R, Chen, I-Ming L., Robinson, Blaine W., Moukarzel, Lea, Cao, Kajia, Devidas, Meenakshi, Carroll, Andrew J., Heerema, Nyla A., Hunger, Stephen, Reaman, Gregory H., Hilden, Joanne M., Camitta, Bruce, Winick, Naomi, Carroll, William L., Zhang, Alena Y., Cory, Lori, Mc Veigh, Steven, Barrett, Jeffery S., Dreyer, Zoann E., Willman, Cheryl L., Felix, Carolyn A.
Published in Blood (19.11.2010)
Published in Blood (19.11.2010)
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Genome Analysis of Thinopyrum intermedium and Its Potential Progenitor Species Using Oligo-FISH
Qi, Fei, Liang, Shuang, Xing, Piyi, Bao, Yinguang, Wang, Richard R.-C., Li, Xingfeng
Published in Plants (Basel) (27.10.2023)
Published in Plants (Basel) (27.10.2023)
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The consequences of chromosomal aneuploidy on gene expression profiles in a cell line model for prostate carcinogenesis
PHILLIPS, John L, HAYWARD, Simon W, LINEHAN, W. Marston, CUNHA, Gerald R, RIED, Thomas, YUZHUO WANG, VASSELLI, James, PAVLOVICH, Christian, PADILLA-NASH, Hesed, PEZULLO, John R, GHADIMI, B. Michael, GROSSFELD, Gary D, RIVERA, Alexandra
Published in Cancer research (Chicago, Ill.) (15.11.2001)
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Published in Cancer research (Chicago, Ill.) (15.11.2001)
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Is There a Yet Unreported Unbalanced Chromosomal Abnormality without Phenotypic Consequences in Proximal 4p?
Liehr, T., Bartels, I., Zoll, B., Ewers, E., Mrasek, K., Kosyakova, N., Merkas, M., Hamid, A.B., von Eggeling, F., Posorski, N., Weise, A.
Published in Cytogenetic and genome research (01.01.2011)
Published in Cytogenetic and genome research (01.01.2011)
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Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14
Ungaro, Paola, Christian, Susan L, Fantes, Judy A, Mutirangura, Apiwat, Black, Susan, Reynolds, James, Malcolm, Sue, Dobyns, William B, Ledbetter, David H
Published in Journal of medical genetics (01.01.2001)
Published in Journal of medical genetics (01.01.2001)
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10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences
Liehr, T., Stumm, M., Wegner, R.D., Bhatt, S., Hickmann, P., Patsalis, P.C., Meins, M., Morlot, S., Klaschka, V., Ewers, E., Hinreiner, S., Mrasek, K., Kosyakova, N., Cai, W.W., Cheung, S.W., Weise, A.
Published in Cytogenetic and genome research (01.01.2009)
Published in Cytogenetic and genome research (01.01.2009)
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The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations
Khan, Abdul Waheed, Kennedy, Alyssa, Furutani, Elissa, Myers, Kasiani, Frattini, Annalisa, Acquati, Francesco, Roccia, Pamela, Micheloni, Giovanni, Minelli, Antonella, Porta, Giovanni, Cipolli, Marco, Cesaro, Simone, Danesino, Cesare, Pasquali, Francesco, Shimamura, Akiko, Valli, Roberto
Published in Molecular cytogenetics (24.11.2021)
Published in Molecular cytogenetics (24.11.2021)
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