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23. Prenatal diagnosis of ATR-X syndrome in a fetus with a new G>T splicing mutation in the XNP/ATR-X gene. Fichera M; Silengo M; Spalletta A; Giudice ML; Romano C; Ragusa A Prenat Diagn; 2001 Sep; 21(9):747-51. PubMed ID: 11559911 [TBL] [Abstract][Full Text] [Related]
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32. Subtelomeric analysis detects a familial 10p;12p rearrangement in two relatives with a distinct syndrome. Battaglia A; Novelli A; Ceccarini C; Bernardini L; Carey JC Am J Med Genet A; 2007 Jan; 143A(2):184-8. PubMed ID: 17163546 [TBL] [Abstract][Full Text] [Related]
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35. De novo 16p deletion: ATR-16 syndrome. Lindor NM; Valdes MG; Wick M; Thibodeau SN; Jalal S Am J Med Genet; 1997 Nov; 72(4):451-4. PubMed ID: 9375730 [TBL] [Abstract][Full Text] [Related]
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37. Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications. Wolfe K; McQuillin A; Alesi V; Boudry Labis E; Cutajar P; Dallapiccola B; Dentici ML; Dieux-Coeslier A; Duban-Bedu B; Duelund Hjortshøj T; Goel H; Loddo S; Morrogh D; Mosca-Boidron AL; Novelli A; Olivier-Faivre L; Parker J; Parker MJ; Patch C; Pelling AL; Smol T; Tümer Z; Vanakker O; van Haeringen A; Vanlerberghe C; Strydom A; Skuse D; Bass N Am J Med Genet B Neuropsychiatr Genet; 2018 Jun; 177(4):397-405. PubMed ID: 29603867 [TBL] [Abstract][Full Text] [Related]
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