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63. A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features. Boudry-Labis E; Demeer B; Le Caignec C; Isidor B; Mathieu-Dramard M; Plessis G; George AM; Taylor J; Aftimos S; Wiemer-Kruel A; Kohlhase J; Annerén G; Firth H; Simonic I; Vermeesch J; Thuresson AC; Copin H; Love DR; Andrieux J Eur J Med Genet; 2013 Mar; 56(3):163-70. PubMed ID: 23279911 [TBL] [Abstract][Full Text] [Related]
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68. Clinical comparison of overlapping deletions of 19p13.3. Risheg H; Pasion R; Sacharow S; Proud V; Immken L; Schwartz S; Tepperberg JH; Papenhausen P; Tan TY; Andrieux J; Plessis G; Amor DJ; Keitges EA Am J Med Genet A; 2013 May; 161A(5):1110-6. PubMed ID: 23610052 [TBL] [Abstract][Full Text] [Related]
69. Clinical characteristics in patients with interstitial deletions of chromosome region 12q21-q22 and identification of a critical region associated with keratosis pilaris. Al-Maawali A; Marshall CR; Scherer SW; Dupuis L; Mendoza-Londono R; Stavropoulos DJ Am J Med Genet A; 2014 Mar; 164A(3):796-800. PubMed ID: 24375972 [TBL] [Abstract][Full Text] [Related]
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76. Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes. Rosenfeld JA; Stephens LE; Coppinger J; Ballif BC; Hoo JJ; French BN; Banks VC; Smith WE; Manchester D; Tsai AC; Merrion K; Mendoza-Londono R; Dupuis L; Schultz R; Torchia B; Sahoo T; Bejjani B; Weaver DD; Shaffer LG Eur J Hum Genet; 2011 May; 19(5):547-54. PubMed ID: 21248749 [TBL] [Abstract][Full Text] [Related]
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