Below are the most recent publications written about "Chromosomes, Human, Pair 13" by people in Profiles.
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Magro G, Angelico G, Righi A, Benini S, Salvatorelli L, Palazzo J. Utility of STAT6 and 13q14 deletion in the classification of the benign spindle cell stromal tumors of the breast. Hum Pathol. 2018 11; 81:55-64.
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Bock F, Lu G, Srour SA, Gaballa S, Lin HY, Baladandayuthapani V, Honhar M, Stich M, Shah ND, Bashir Q, Patel K, Popat U, Hosing C, Korbling M, Delgado R, Rondon G, Shah JJ, Thomas SK, Manasanch EE, Isermann B, Orlowski RZ, Champlin RE, Qazilbash MH. Outcome of Patients with Multiple Myeloma and CKS1B Gene Amplification after Autologous Hematopoietic Stem Cell Transplantation. Biol Blood Marrow Transplant. 2016 12; 22(12):2159-2164.
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Uwineza A, Hitayezu J, Jamar M, Caberg JH, Murorunkwere S, Janvier N, Bours V, Mutesa L. Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies. J Trop Pediatr. 2016 Feb; 62(1):38-45.
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Uwineza A, Pierquin G, Gaillez S, Jamar M, Hellin AC, Caberg JH, Bours V. Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13. Genet Couns. 2013; 24(2):193-200.
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Der Kaloustian VM, Russell L, Aradhya S, Richard G, Rosenblatt B, Melan?on S. A de novo 2.1-Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic features. Am J Med Genet A. 2011 Oct; 155A(10):2538-42.
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Fabbri M, Bottoni A, Shimizu M, Spizzo R, Nicoloso MS, Rossi S, Barbarotto E, Cimmino A, Adair B, Wojcik SE, Valeri N, Calore F, Sampath D, Fanini F, Vannini I, Musuraca G, Dell'Aquila M, Alder H, Davuluri RV, Rassenti LZ, Negrini M, Nakamura T, Amadori D, Kay NE, Rai KR, Keating MJ, Kipps TJ, Calin GA, Croce CM. Association of a microRNA/TP53 feedback circuitry with pathogenesis and outcome of B-cell chronic lymphocytic leukemia. JAMA. 2011 Jan 05; 305(1):59-67.
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Bornstein E, Barnhard Y, Donnenfeld A, Ferber A, Divon MY. Fetal pyelectasis: does fetal gender modify the risk of major trisomies? Obstet Gynecol. 2006 Apr; 107(4):877-9.
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Shields CL, Shields JA. Diagnosis and management of retinoblastoma. Cancer Control. 2004 Sep-Oct; 11(5):317-27.
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Hyytinen ER, Frierson HF, Sipe TW, Li CL, Degeorges A, Sikes RA, Chung LW, Dong JT. Loss of heterozygosity and lack of mutations of the XPG/ERCC5 DNA repair gene at 13q33 in prostate cancer. Prostate. 1999 Nov 01; 41(3):190-5.
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Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L, Mansfield E, Rappaport E, Govea N, Mil? M, Zelante L, Gasparini P. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet. 1998 Feb 07; 351(9100):394-8.