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	1081.	Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita. [electronic resource] by Parry, Erin M Alder, Jonathan K Lee, Stella S Phillips, John A Loyd, James E Duggal, Priya Armanios, Mary Producer: 20110826 In: Journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1082.	X chromosome inactivation in human parthenogenetic embryonic stem cells following prolonged passaging. [electronic resource] by Qi, Quan Ding, Chenhui Hong, Pingping Yang, Gang Xie, Yanxin Wang, Jing Huang, Sunxing He, Ke Zhou, Canquan Producer: 20151005 In: International journal of molecular medicine vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1083.	Duplication at Xq13.3-q21.1 with syndromic intellectual disability, a probable role for the ATRX gene. [electronic resource] by Martínez, Francisco Roselló, Mónica Mayo, Sonia Monfort, Sandra Oltra, Silvestre Orellana, Carmen Producer: 20141215 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1084.	The State of Skewed X Chromosome Inactivation is Retained in the Induced Pluripotent Stem Cells from a Female with Hemophilia B. [electronic resource] by Lyu, Cuicui Shen, Jun Zhang, Jianping Xue, Feng Liu, Xiaofan Liu, Wei Fu, Rongfeng Zhang, Liyan Li, Huiyuan Zhang, Donglei Zhang, Xiaobing Cheng, Tao Yang, Renchi Zhang, Lei Producer: 20180321 In: Stem cells and development vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1085.	Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations. [electronic resource] by Suzuki, Erina Shima, Hirohito Toki, Machiko Hanew, Kunihiko Matsubara, Keiko Kurahashi, Hiroki Narumi, Satoshi Ogata, Tsutomu Kamimaki, Tsutomu Fukami, Maki Producer: 20170221 In: Cytogenetic and genome research vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1086.	Large Duplications Can Be Benign Copy Number Variants: A Case of a 3.6-Mb Xq21.33 Duplication. [electronic resource] by Maurin, Marie-Laure Arfeuille, Chloé Sonigo, Pascale Rondeau, Sophie Vekemans, Michel Turleau, Catherine Ville, Yves Malan, Valérie Producer: 20170914 In: Cytogenetic and genome research vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1087.	Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation. [electronic resource] by Bacher, Christian P Guggiari, Michèle Brors, Benedikt Augui, Sandrine Clerc, Philippe Avner, Philip Eils, Roland Heard, Edith Producer: 20060501 In: Nature cell biology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1088.	Differential X reactivation in human placental cells: implications for reversal of X inactivation. [electronic resource] by Migeon, Barbara R Axelman, Joyce Jeppesen, Peter Producer: 20060206 In: American journal of human genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1089.	A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome. [electronic resource] by Cau, Milena Addis, Maria Congiu, Rita Meloni, Cristiana Cao, Antonio Santaniello, Simona Loi, Mario Emma, Francesco Zuffardi, Orsetta Ciccone, Roberto Sole, Gabriella Melis, Maria Antonietta Producer: 20070117 In: Journal of human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1090.	Dosage compensation on the active X chromosome minimizes transcriptional noise of X-linked genes in mammals. [electronic resource] by Yin, Shanye Wang, Ping Deng, Wenjun Zheng, Hancheng Hu, Landian Hurst, Laurence D Kong, Xiangyin Producer: 20100113 In: Genome biology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1091.	Occurrence of 47,X,i(X)(q10),Y Klinefelter variant with hypogonadotropic hypogonadism. [electronic resource] by Sabbaghian, Marjan Meybodi, Anahita Mohseni Rahimian, Mouness Sadighi Gilani, Mohammad Ali Producer: 20110926 In: Fertility and sterility vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1092.	X-linked thrombocytopenia in a female with a complex familial pattern of X-chromosome inactivation. [electronic resource] by Daza-Cajigal, V Martínez-Pomar, N Garcia-Alonso, A Heine-Suñer, D Torres, S Vega, A K Molina, I J Matamoros, N Producer: 20140109 In: Blood cells, molecules & diseases vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1093.	X marks the spot: does it matter that O-GlcNAc transferase is an X-linked gene? [electronic resource] by Olivier-Van Stichelen, Stéphanie Abramowitz, Lara K Hanover, John A Producer: 20150213 In: Biochemical and biophysical research communications vol. 453 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1094.	Familial cases and male cases with MECP2 mutations. [electronic resource] by Zhang, Qingping Zhao, Ying Bao, Xinhua Luo, Jinjun Zhang, Xiaoying Li, Jiarui Wei, Liping Wu, Xiru Producer: 20180207 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 174 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1095.	Effects of the HDAC inhibitor scriptaid on the in vitro development of bovine embryos and on imprinting gene expression levels. [electronic resource] by Laguna-Barraza, R Sánchez-Calabuig, M J Gutiérrez-Adán, A Rizos, D Pérez-Cerezales, S Producer: 20180924 In: Theriogenology vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1096.	A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma. [electronic resource] by Ouyang, Pingbo Li, Yun Zhang, Feng Zhu, Chengzhang Zou, Beiji Le, Jianlan Zhang, Lusi Producer: 20180926 In: Molecular medicine reports vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1097.	Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. [electronic resource] by Rauch, Anita Hoyer, Juliane Guth, Sabine Zweier, Christiane Kraus, Cornelia Becker, Christian Zenker, Martin Hüffmeier, Ulrike Thiel, Christian Rüschendorf, Franz Nürnberg, Peter Reis, André Trautmann, Udo Producer: 20061129 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1098.	Histogenesis of clear cell adenocarcinoma in the urinary tract: evidence of urothelial origin. [electronic resource] by Sung, Ming-Tse Zhang, Shaobo MacLennan, Gregory T Lopez-Beltran, Antonio Montironi, Rodolfo Wang, Mingsheng Tan, Puay-Hoon Cheng, Liang Producer: 20080624 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1099.	Low burden of a JAK2-V617F mutated clone in monoclonal haematopoiesis in a Japanese woman with Budd-Chiari syndrome. [electronic resource] by Toyama, Kohtaro Karasawa, Masamitsu Yamane, Arito Koiso, Hiromi Yokohama, Akihiko Uchiumi, Hideki Saitoh, Takayuki Handa, Hiroshi Sato, Ken Takagi, Hitoshi Miyawaki, Shuichi Murakami, Hirokazu Nojima, Yoshihisa Tsukamoto, Norifumi Producer: 20090622 In: International journal of hematology vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1100.	Stage-specific expression profiling of Drosophila spermatogenesis suggests that meiotic sex chromosome inactivation drives genomic relocation of testis-expressed genes. [electronic resource] by Vibranovski, Maria D Lopes, Hedibert F Karr, Timothy L Long, Manyuan Producer: 20100302 In: PLoS genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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