PMC Articles for MedGen (Select 436306) - PMC

Select item 53557371.

Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature

Shaobin Lin, Yi Zhou, Qun Fang, Jianzhu Wu, Zhiqiang Zhang, Yuanjun Ji, Yanmin Luo

Mol Med Rep. 2016 Dec; 14(6): 5134–5140. Published online 2016 Oct 19. doi: 10.3892/mmr.2016.5864

PMCID:: PMC5355737

Select item 54092172.

MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion

Laura Fontana, Silvia Tabano, Eleonora Bonaparte, Giovanni Marfia, Chiara Pesenti, Rossella Falcone, Claudia Augello, Nicole Carlessi, Rosamaria Silipigni, Silvana Guerneri, Rolando Campanella, Manuela Caroli, Silvia Maria Sirchia, Silvano Bosari, Monica Miozzo

J Neuropathol Exp Neurol. 2016 Aug; 75(8): 791–800. Published online 2016 Jun 24. doi: 10.1093/jnen/nlw052

PMCID:: PMC5409217

Abstract Article PDF–843K

Select item 10159563.

Monosomy 10qter: a new case.

M Teyssier, C Charrin, J Dutruge, C Rousselle

J Med Genet. 1992 May; 29(5): 342–343. doi: 10.1136/jmg.29.5.342

PMCID:: PMC1015956

Summary Page Browse PDF–338K

Select item 60487984.

Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case report

Ruen Yao, Tingting Yu, Yufei Xu, Guoqiang Li, Lei Yin, Yunfang Zhou, Jian Wang, Zhilong Yan

BMC Med Genomics. 2018; 11: 60. Published online 2018 Jul 16. doi: 10.1186/s12920-018-0377-3

PMCID:: PMC6048798

Abstract Article PDF–722K

Select item 51934695.

Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines

Karine Michaud, Marie de Tayrac, Myreille D’Astous, Céline Duval, Claudie Paquet, Oumar Samassekou, Peter Vincent Gould, Stéphan Saikali

PLoS One. 2016; 11(12): e0168728. Published online 2016 Dec 28. doi: 10.1371/journal.pone.0168728

PMCID:: PMC5193469

Abstract Article PDF–2.2M

Select item 45383276.

Pediatric and adult sonic hedgehog medulloblastomas are clinically and molecularly distinct

Paul A. Northcott, Thomas Hielscher, Adrian Dubuc, Stephen Mack, David Shih, Marc Remke, Hani Al-Halabi, Steffen Albrecht, Nada Jabado, Charles G. Eberhart, Wieslawa Grajkowska, William A. Weiss, Steven C. Clifford, Eric Bouffet, James T. Rutka, Andrey Korshunov, Stefan Pfister, Michael D. Taylor

Acta Neuropathol. Author manuscript; available in PMC 2015 Aug 17.

Published in final edited form as: Acta Neuropathol. 2011 Aug; 122(2): 231–240. Published online 2011 Jun 17. doi: 10.1007/s00401-011-0846-7

PMCID:: PMC4538327

Abstract Article PDF–715K

Select item 38307497.

TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma

Marc Remke, Vijay Ramaswamy, John Peacock, David J. H. Shih, Christian Koelsche, Paul A. Northcott, Nadia Hill, Florence M. G. Cavalli, Marcel Kool, Xin Wang, Stephen C. Mack, Mark Barszczyk, A. Sorana Morrissy, Xiaochong Wu, Sameer Agnihotri, Betty Luu, David T. W. Jones, Livia Garzia, Adrian M. Dubuc, Nataliya Zhukova, Robert Vanner, Johan M. Kros, Pim J. French, Erwin G. Van Meir, Rajeev Vibhakar, Karel Zitterbart, Jennifer A. Chan, László Bognár, Almos Klekner, Boleslaw Lach, Shin Jung, Ali G. Saad, Linda M. Liau, Steffen Albrecht, Massimo Zollo, Michael K. Cooper, Reid C. Thompson, Oliver O. Delattre, Franck Bourdeaut, François F. Doz, Miklós Garami, Peter Hauser, Carlos G. Carlotti, Timothy E. Van Meter, Luca Massimi, Daniel Fults, Scott L. Pomeroy, Toshiro Kumabe, Young Shin Ra, Jeffrey R. Leonard, Samer K. Elbabaa, Jaume Mora, Joshua B. Rubin, Yoon-Jae Cho, Roger E. McLendon, Darell D. Bigner, Charles G. Eberhart, Maryam Fouladi, Robert J. Wechsler-Reya, Claudia C. Faria, Sidney E. Croul, Annie Huang, Eric Bouffet, Cynthia E. Hawkins, Peter B. Dirks, William A. Weiss, Ulrich Schüller, Ian F. Pollack, Stefan Rutkowski, David Meyronet, Anne Jouvet, Michelle Fèvre-Montange, Nada Jabado, Marta Perek-Polnik, Wieslawa A. Grajkowska, Seung-Ki Kim, James T. Rutka, David Malkin, Uri Tabori, Stefan M. Pfister, Andrey Korshunov, Andreas von Deimling, Michael D. Taylor

Acta Neuropathol. 2013; 126(6): 917–929. Published online 2013 Oct 31. doi: 10.1007/s00401-013-1198-2

PMCID:: PMC3830749

Abstract Article PDF–800K

Select item 10155398.

A case of interstitial deletion of 10q25.2----q26.1.

D E Rooney, K Williams, D V Coleman, A Habel

J Med Genet. 1989 Jan; 26(1): 58–60. doi: 10.1136/jmg.26.1.58

PMCID:: PMC1015539

Summary Page Browse PDF–485K

Select item 43523609.

Prenatal diagnosis of trisomy 6q25.3-qter and monosomy 10q26.12-qter by array CGH in a fetus with an apparently normal karyotype

Ponnila S Marinescu, Devereux N Saller, W Tony Parks, Svetlana A Yatsenko, Aleksandar Rajkovic

Clin Case Rep. 2015 Feb; 3(2): 92–95. Published online 2014 Oct 15. doi: 10.1002/ccr3.162

PMCID:: PMC4352360

Abstract Article PDF–615K

Select item 730007810.

Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion

Anudeep Yekula, Connor Grant, Mihir Gupta, David R. Santiago-Dieppa, Pate J. Duddleston, David Gonda, Michael Levy

Childs Nerv Syst. 2020; 36(7): 1367–1377. Published online 2020 May 12. doi: 10.1007/s00381-020-04642-2

PMCID:: PMC7300078

Abstract Article PDF–523K

Select item 481961811.

Private rare deletions in SEC16A and MAMDC4 may represent novel pathogenic variants in familial axial spondyloarthritis

Darren D O'Rielly, Mohammed Uddin, Dianne Codner, Michael Hayley, Jiayi Zhou, Lourdes Pena-Castillo, Ahmed A Mostafa, S M Mahmudul Hasan, William Liu, Nigil Haroon, Robert Inman, Proton Rahman

Ann Rheum Dis. 2016 Apr; 75(4): 772–779. Published online 2015 May 8. doi: 10.1136/annrheumdis-2014-206484

PMCID:: PMC4819618

Abstract Article PDF–1.2M

Select item 419585512.

Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas

Hinke F van Thuijl, Ilari Scheinin, Daoud Sie, Agusti Alentorn, Hendrik F van Essen, Martijn Cordes, Ruth Fleischeuer, Anja M Gijtenbeek, Guus Beute, Wimar A van den Brink, Gerrit A Meijer, Miek Havenith, Ahmed Idbaih, Khê Hoang-Xuan, Karima Mokhtari, Roel GW Verhaak, Paul van der Valk, Mark A van de Wiel, Jan J Heimans, Eleonora Aronica, Jaap C Reijneveld, Pieter Wesseling, Bauke Ylstra

Genome Biol. 2014; 15(9): 471. Published online 2014 Sep 23. doi: 10.1186/s13059-014-0471-6

PMCID:: PMC4195855

Abstract Article PDF–1.8M

Select item 360665313.

An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma

Hassan M. Minhas, Matthew F. Pescosolido, Matthew Schwede, Justyna Piasecka, John Gaitanis, Umadevi Tantravahi, Eric M. Morrow

Am J Med Genet A. Author manuscript; available in PMC 2014 Apr 1.

Published in final edited form as: Am J Med Genet A. 2013 Apr; 161(4): 787–791. Published online 2013 Mar 12. doi: 10.1002/ajmg.a.35841

PMCID:: PMC3606653

Abstract Article PDF–790K

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