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31. Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region. Nickel RE; Pillers DA; Merkens M; Magenis RE; Driscoll DA; Emanuel BS; Zonana J Eur J Pediatr Surg; 1993 Dec; 3 Suppl 1():27-8. PubMed ID: 8130147 [No Abstract] [Full Text] [Related]
32. 22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features. Burnside RD Cytogenet Genome Res; 2015; 146(2):89-99. PubMed ID: 26278718 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2? Wulfsberg EA Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634 [No Abstract] [Full Text] [Related]
35. 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome. Ben-Shachar S; Ou Z; Shaw CA; Belmont JW; Patel MS; Hummel M; Amato S; Tartaglia N; Berg J; Sutton VR; Lalani SR; Chinault AC; Cheung SW; Lupski JR; Patel A Am J Hum Genet; 2008 Jan; 82(1):214-21. PubMed ID: 18179902 [TBL] [Abstract][Full Text] [Related]
36. The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications. Vantrappen G; Rommel N; Cremers CW; Devriendt K; Frijns JP Int J Pediatr Otorhinolaryngol; 1998 Oct; 45(2):133-41. PubMed ID: 9849681 [TBL] [Abstract][Full Text] [Related]