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2. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome]. Pânzaru M; Rusu C; Voloşciuc M; Braha E; Butnariu L; Ivanov I; Grămescu M; Popescu R; Caba L; Sireteanu A; Macovei M; Covic M; Gorduza EV Rev Med Chir Soc Med Nat Iasi; 2011; 115(3):756-61. PubMed ID: 22046783 [TBL] [Abstract][Full Text] [Related]
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6. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features. Kitsiou-Tzeli S; Kolialexi A; Fryssira H; Galla-Voumvouraki A; Salavoura K; Kanariou M; Tsangaris GT; Kanavakis E; Mavrou A In Vivo; 2004; 18(5):603-8. PubMed ID: 15523900 [TBL] [Abstract][Full Text] [Related]
7. [22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis]. Ingrao T; Lambert L; Valduga M; Bosser G; Albuisson E; Leheup B Arch Pediatr; 2017 Nov; 24(11):1067-1075. PubMed ID: 28967605 [TBL] [Abstract][Full Text] [Related]
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12. Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome. Gothelf D; Feinstein C; Thompson T; Gu E; Penniman L; Van Stone E; Kwon H; Eliez S; Reiss AL Am J Psychiatry; 2007 Apr; 164(4):663-9. PubMed ID: 17403981 [TBL] [Abstract][Full Text] [Related]
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20. The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome. Van Esch H; Groenen P; Fryns JP; Van de Ven W; Devriendt K Genet Couns; 1999; 10(1):59-65. PubMed ID: 10191430 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]