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Journal Abstract Search
338 related items for PubMed ID: 10191429
1. The deletions of 22q11--the Portuguese experience. Gaspar IM, Lourenço MT, Reis MI, Soares MA, Nogueira G, Ferreira F, Feijóo MJ. Genet Couns; 1999; 10(1):51-7. PubMed ID: 10191429 [Abstract] [Full Text] [Related]
2. Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11. Marino B, Digilio MC, Toscano A, Giannotti A, Dallapiccola B. Genet Couns; 1999; 10(1):25-33. PubMed ID: 10191426 [Abstract] [Full Text] [Related]
11. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects. Hou JW, Wang JK, Tsai WY, Chou CC, Wang TR. J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164 [Abstract] [Full Text] [Related]
14. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot]. Morava E, Masszi G, Czakó M, Tóth G, Melegh B, Kosztolányi G. Orv Hetil; 2000 Aug 20; 141(34):1873-5. PubMed ID: 11006712 [Abstract] [Full Text] [Related]
15. [CATCH22 or 22q11 deletion syndrome. An underdiagnosed and misunderstood disease category with a variable clinical picture]. Oskarsdóttir S, Fasth A, Belfrage M, Viggedal G, Persson C, Eriksson BO. Lakartidningen; 1999 Nov 03; 96(44):4789-93. PubMed ID: 10584540 [Abstract] [Full Text] [Related]