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	141.	LETM1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this condition. [electronic resource] by Hart, Lesley Rauch, Anita Carr, Antony M Vermeesch, Joris R O'Driscoll, Mark Producer: 20141217 In: Disease models & mechanisms vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	142.	4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions. [electronic resource] by Bi, Weimin Cheung, Sau-Wai Breman, Amy M Bacino, Carlos A Producer: 20171019 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	143.	Melatonin reverses the oxidative stress and mitochondrial dysfunction caused by LETM1 silencing. [electronic resource] by Aral, Cenk Demirkesen, Seyma Bircan, Rıfat Yasar Sirin, Duygu Producer: 20200930 In: Cell biology international vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	144.	[Wolf-Hirschhorn syndrome. A series of 27 patients: their epidemiological and clinical characteristics. The current situation of the patients and the opinions of their caregivers regarding the diagnostic process]. [electronic resource] by Blanco-Lago, Raquel Málaga, Ignacio García-Peñas, Juan José García-Ron, Adrián Producer: 20140203 In: Revista de neurologia vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	145.	Wolf-Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions. [electronic resource] by Engbers, Hannelie van der Smagt, Jasper J van 't Slot, Ruben Vermeesch, Joris R Hochstenbach, Ron Poot, Martin Producer: 20090205 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	146.	Evaluation of polymorphisms in predicted target sites for micro RNAs differentially expressed in endometriosis. [electronic resource] by Zhao, Zhen Zhen Croft, Larry Nyholt, Dale R Chapman, Brett Treloar, Susan A Hull, M Louise Montgomery, Grant W Producer: 20110505 In: Molecular human reproduction vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	147.	[Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization]. [electronic resource] by Zhu, Chun-jiang Huang, Zhi-yun Wu, Wei-qing Zhao, Qin Jiang, Hai-yan Xie, Jian-sheng Producer: 20130314 In: Zhonghua er ke za zhi = Chinese journal of pediatrics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	148.	Wolf-Hirschhorn Syndrome Candidate 1 (whsc1) Functions as a Tumor Suppressor by Governing Cell Differentiation. [electronic resource] by Yu, Chuan Yao, Xiaomin Zhao, Linjie Wang, Ping Zhang, Qian Zhao, Chengjian Yao, Shaohua Wei, Yuquan Producer: 20180406 In: Neoplasia (New York, N.Y.) vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	149.	C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development. [electronic resource] by Endele, Sabine Nelkenbrecher, Claudia Bördlein, Annegret Schlickum, Stefanie Winterpacht, Andreas Producer: 20110916 In: Neurogenetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	150.	Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones. [electronic resource] by Chen, Chih-Ping Chen, Chen-Yu Chern, Schu-Rern Wu, Peih-Shan Chen, Shin-Wen Lai, Shih-Ting Chuang, Tzu-Yun Yang, Chien-Wen Chen, Li-Feng Wang, Wayseen Producer: 20180801 In: Taiwanese journal of obstetrics & gynecology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	151.	Cell biology. A revolving door for calcium. [electronic resource] by Demaurex, Nicolas Poburko, Damon Producer: 20091016 In: Science (New York, N.Y.) vol. 326 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	152.	Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16. [electronic resource] by Zollino, Marcella Lecce, Rosetta Murdolo, Marina Orteschi, Daniela Marangi, Giuseppe Selicorni, Angelo Midro, Alina Sorge, Giovanni Zampino, Giuseppe Memo, Luigi Battaglia, Domenica Petersen, Michael Pandelia, Effie Gyftodimou, Yolanda Faravelli, Francesca Tenconi, Romano Garavelli, Livia Mazzanti, Laura Fischetto, Rita Cavalli, Pietro Savasta, Salvatore Rodriguez, Laura Neri, Giovanni Producer: 20080416 In: Human genetics vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	153.	Trisomy 12p and monosomy 4p: phenotype-genotype correlation. [electronic resource] by Benussi, Daniela Gambel Costa, Paola Zollino, Marcella Murdolo, Marina Petix, Vincenzo Carrozzi, Marco Pecile, Vanna Producer: 20090709 In: Genetic testing and molecular biomarkers vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	154.	Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype. [electronic resource] by South, Sarah T Whitby, Heidi Maxwell, Teresa Aston, Emily Brothman, Arthur R Carey, John C Producer: 20081112 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)
	155.	The histone methyltransferase MMSET regulates class switch recombination. [electronic resource] by Pei, Huadong Wu, Xiaosheng Liu, Tongzheng Yu, Kefei Jelinek, Diane F Lou, Zhenkun Producer: 20130314 In: Journal of immunology (Baltimore, Md. : 1950) vol. 190 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	156.	Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: experience with 87 patients. [electronic resource] by Battaglia, Agatino Filippi, Tiziana South, Sarah T Carey, John C Producer: 20090504 In: Developmental medicine and child neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	157.	109 kb deletion of chromosome 4p16.3 in a patient with mild phenotype of Wolf-Hirschhorn syndrome. [electronic resource] by Okamoto, Nobuhiko Ohmachi, Kazumi Shimada, Shino Shimojima, Keiko Yamamoto, Toshiyuki Producer: 20160415 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	158.	Letm1, the mitochondrial Ca2+/H+ antiporter, is essential for normal glucose metabolism and alters brain function in Wolf-Hirschhorn syndrome. [electronic resource] by Jiang, Dawei Zhao, Linlin Clish, Clary B Clapham, David E Producer: 20130823 In: Proceedings of the National Academy of Sciences of the United States of America vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	159.	Multiple congenital malformations of Wolf-Hirschhorn syndrome are recapitulated in Fgfrl1 null mice. [electronic resource] by Catela, Catarina Bilbao-Cortes, Daniel Slonimsky, Esfir Kratsios, Paschalis Rosenthal, Nadia Te Welscher, Pascal Producer: 20090715 In: Disease models & mechanisms vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	160.	Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome. [electronic resource] by Hammond, Peter Hannes, Femke Suttie, Michael Devriendt, Koen Vermeesch, Joris Robert Faravelli, Francesca Forzano, Francesca Parekh, Susan Williams, Steve McMullan, Dominic South, Sarah T Carey, John C Quarrell, Oliver Producer: 20120402 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 163 results.