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	1401.	Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome. [electronic resource] by van Rahden, Vanessa A Fernandez-Vizarra, Erika Alawi, Malik Brand, Kristina Fellmann, Florence Horn, Denise Zeviani, Massimo Kutsche, Kerstin Producer: 20150529 In: American journal of human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1402.	The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. [electronic resource] by Vandewalle, Joke Bauters, Marijke Van Esch, Hilde Belet, Stefanie Verbeeck, Jelle Fieremans, Nathalie Holvoet, Maureen Vento, Jodie Spreiz, Ana Kotzot, Dieter Haberlandt, Edda Rosenfeld, Jill Andrieux, Joris Delobel, Bruno Dehouck, Marie-Bertille Devriendt, Koen Fryns, Jean-Pierre Marynen, Peter Goldstein, Amy Froyen, Guy Producer: 20131104 In: Human genetics vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1403.	Live-cell imaging combined with immunofluorescence, RNA, or DNA FISH to study the nuclear dynamics and expression of the X-inactivation center. [electronic resource] by Pollex, Tim Piolot, Tristan Heard, Edith Producer: 20140331 In: Methods in molecular biology (Clifton, N.J.) vol. 1042 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1404.	A small and active ring X chromosome in a female with features of Kabuki syndrome. [electronic resource] by Rodríguez, L Diego-Alvarez, D Lorda-Sanchez, I Gallardo, F L Martínez-Fernández, M L Arroyo-Muñoz, M E Martínez-Frías, M L Producer: 20081209 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1405.	The Xp contiguous deletion syndrome and autism. [electronic resource] by Shinawi, Marwan Patel, Ankita Panichkul, Prisana Zascavage, Roxanne Peters, Sarika U Scaglia, Fernando Producer: 20090730 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1406.	Large genomic rearrangements in MECP2. [electronic resource] by Ravn, Kirstine Nielsen, Jytte Bieber Skjeldal, Ola Husbeth Kerr, Alison Hulten, Maj Schwartz, Marianne Producer: 20060516 In: Human mutation vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1407.	A new missense mutation found in the FLNA gene in a family with bilateral periventricular nodular heterotopia (BPNH) alters the splicing process. [electronic resource] by Tsuneda, Simone S Torres, Fabio R Montenegro, Maria A Guerreiro, Marilisa M Cendes, Fernando Lopes-Cendes, Iscia Producer: 20080822 In: Journal of molecular neuroscience : MN vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1408.	Xist repression shows time-dependent effects on the reprogramming of female somatic cells to induced pluripotent stem cells. [electronic resource] by Chen, Qi Gao, Shuai He, Wenteng Kou, Xiaochen Zhao, Yanhong Wang, Hong Gao, Shaorong Producer: 20150520 In: Stem cells (Dayton, Ohio) vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1409.	A novel mutation in SOX3 polyalanine tract: a case of Kabuki syndrome with combined pituitary hormone deficiency harboring double mutations in MLL2 and SOX3. [electronic resource] by Takagi, Masaki Ishii, Tomohiro Torii, Chiharu Kosaki, Kenjiro Hasegawa, Tomonobu Producer: 20150701 In: Pituitary vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1410.	Variability of sexual phenotype in 46,XX(SRY+) patients: the influence of spreading X inactivation versus position effects. [electronic resource] by Sharp, A Kusz, K Jaruzelska, J Tapper, W Szarras-Czapnik, M Wolski, J Jacobs, P Producer: 20060417 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1411.	Molecular evidence for the same clonal origin of multifocal papillary thyroid carcinomas. [electronic resource] by McCarthy, Ryan P Wang, Mingsheng Jones, Timothy D Strate, Randall W Cheng, Liang Producer: 20061030 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1412.	Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseases. [electronic resource] by Douvaras, Panagiotis Liu, Weijia Mort, Richard L McKie, Lisa West, Katrine M Cross, Sally H Morley, Steven D West, John D Producer: 20130110 In: BMC research notes vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1413.	Genetic and epigenetic X-chromosome variations in a parthenogenetic human embryonic stem cell line. [electronic resource] by Liu, Weiqiang Yin, Yifei Jiang, Yonghua Kou, Chaohui Luo, Yumei Huang, Shengchang Zheng, Yuhong Li, Shaoying Li, Qing Guo, Liyuan Gao, Shaorong Sun, Xiaofang Producer: 20111017 In: Journal of assisted reproduction and genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1414.	Neuropathological features in a female fetus with OPHN1 deletion and cerebellar hypoplasia. [electronic resource] by Rocas, Delphine Alix, Eudeline Michel, Jessica Cordier, Marie-Pierre Labalme, Audrey Guilbert, Hélène Till, Marianne Schluth-Bolard, Caroline de Haas, Pascale Massardier, Jérôme Portes, Vincent des Edery, Patrick Touraine, Renaud Guibaud, Laurent Vasiljevic, Alexandre Sanlaville, Damien Producer: 20140102 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1415.	Familial skewed x chromosome inactivation in adrenoleukodystrophy manifesting heterozygotes from a Chinese pedigree. [electronic resource] by Wang, Zhihong Yan, Aizhen Lin, Yuxiang Xie, Haihua Zhou, Chunyan Lan, Fenghua Producer: 20130827 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1416.	Analysis of a four generation family reveals the widespread sequence-dependent maintenance of allelic DNA methylation in somatic and germ cells. [electronic resource] by Tang, Aifa Huang, Yi Li, Zesong Wan, Shengqing Mou, Lisha Yin, Guangliang Li, Ning Xie, Jun Xia, Yudong Li, Xianxin Luo, Liya Zhang, Junwen Chen, Shen Wu, Song Sun, Jihua Sun, Xiaojuan Jiang, Zhimao Chen, Jing Li, Yingrui Wang, Jian Wang, Jun Cai, Zhiming Gui, Yaoting Producer: 20161213 In: Scientific reports vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1417.	Smchd1 Targeting to the Inactive X Is Dependent on the Xist-HnrnpK-PRC1 Pathway. [electronic resource] by Jansz, Natasha Nesterova, Tatyana Keniry, Andrew Iminitoff, Megan Hickey, Peter F Pintacuda, Greta Masui, Osamu Kobelke, Simon Geoghegan, Niall Breslin, Kelsey A Willson, Tracy A Rogers, Kelly Kay, Graham F Fox, Archa H Koseki, Haruhiko Brockdorff, Neil Murphy, James M Blewitt, Marnie E Producer: 20191210 In: Cell reports vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1418.	None [electronic resource] by Souyris, Mélanie Cenac, Claire Azar, Pascal Daviaud, Danièle Canivet, Astrid Grunenwald, Solange Pienkowski, Catherine Chaumeil, Julie Mejía, José E Guéry, Jean-Charles Producer: 20181126 In: Science immunology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1419.	Clustered transcripts that escape X inactivation at mouse XqD. [electronic resource] by Lopes, Alexandra M Arnold-Croop, Sarah E Amorim, António Carrel, Laura Producer: 20120117 In: Mammalian genome : official journal of the International Mammalian Genome Society vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1420.	Role of the CAG repeat polymorphism of the androgen receptor gene in polycystic ovary syndrome (PCOS). [electronic resource] by Schüring, A N Welp, A Gromoll, J Zitzmann, M Sonntag, B Nieschlag, E Greb, R R Kiesel, L Producer: 20120601 In: Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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