Digeorge syndrome : New insightsGOLDMUNTZ, Elizabeth.Clinics in perinatology. 2005, Vol 32, Num 4, pp ix-x, issn 0095-5108, 18 p.Article

Cytogenetic findings in a prospective series of patients with DiGeorge anomalyGREENBERG, F; ELDER, F. F. B; HAFFNER, P et al.American journal of human genetics. 1988, Vol 43, Num 5, pp 605-611, issn 0002-9297Article

Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndromeBABCOCK, Melanie; YATSENKO, Svetlana; HOPKINS, Janet et al.Human molecular genetics (Print). 2007, Vol 16, Num 21, pp 2560-2571, issn 0964-6906, 12 p.Article

Causes of the phenotype-genotype dissociation in DiGeorge syndrome: clues from mouse modelsBOTTA, Annalisa; AMATI, Francesca; NOVELLI, Giuseppe et al.Trends in genetics (Regular ed.). 2001, Vol 17, Num 10, pp 551-554, issn 0168-9525Article

Genetic disorders of cardiac morphogenesis : The DiGeorge and velocardiofacial syndromesGOLDMUNTZ, E; EMANUEL, B. S.Circulation research. 1997, Vol 80, Num 4, pp 437-443, issn 0009-7330Article

Transposition of the great arteries associated with deletion of chromosome 22q11MELCHIONDA, S; DIGILIO, M. C; MINGARELLI, R et al.The American journal of cardiology. 1995, Vol 75, Num 1, pp 95-98, issn 0002-9149Article

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndromeSCAMBLER, P. J; CAREY, A. H; WYSE, R. K. H et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 1, pp 201-206, issn 0888-7543, 6 p.Article

Hypogammaglobulinaemia in DiGeorge sequence. ReplyETZIONI, A; POLLACK, S; MAYUMI, M et al.European journal of pediatrics. 1989, Vol 149, Num 2, pp 143-144, issn 0340-6199Article

Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndromeGOTHELF, Doron; FEINSTEIN, Carl; THOMPSON, Tracy et al.The American journal of psychiatry. 2007, Vol 164, Num 4, pp 663-669, issn 0002-953X, 7 p.Article

Congenital vascular tortuosity in digeorge syndrome mimicking significant retinopathy of prematurityHILL, Vivian E; PIETUCHA, Shamek; ELLS, Anna L et al.Archives of ophthalmology (1960). 2004, Vol 122, Num 1, pp 132-133, issn 0003-9950, 2 p.Article

Selective polysaccharide antibody deficiency in familial DiGeorge syndromeSCHUBERT, M. S; MOSS, R. B.Annals of allergy. 1992, Vol 69, Num 3, pp 231-238, issn 0003-4738Conference Paper

Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequenceMASCARELLO, J. T; BASTIAN, J. F; JONES, M. C et al.American journal of medical genetics. 1989, Vol 32, Num 1, pp 112-114, issn 0148-7299, 3 p.Article

The DiGeorge syndrome. I: Clinical evaluation and course of partial and complete forms of the syndromeMÜLLER, W; PETER, H. H; WILKEN, M et al.European journal of pediatrics. 1988, Vol 147, Num 5, pp 496-502, issn 0340-6199Article

DiGeorge anomaly associated with 10p deletionMONACO, G; PIGNATA, C; ROSSI, E et al.American journal of medical genetics. 1991, Vol 39, Num 2, pp 215-216, issn 0148-7299Article

Severe eczema in a patient with DiGeorge's syndromeARCHER, E; TSU-YI CHUANG; HONG, R et al.Cutis (New York, NY). 1990, Vol 45, Num 6, pp 455-459, issn 0011-4162, 5 p.Article

The thymus in congenital heart diseaseHENRIQUES, U. V; DYBDAHL, H.Acta pathologica, microbiologica et immunologica Scandinavica. Section A. Pathology. 1985, Vol 93, Num 2, pp 89-92, issn 0108-0164Article

Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucencyDONNENFELD, Alan E; CUTILLO, Denise; HORWITZ, Juli et al.American journal of obstetrics and gynecology. 2006, Vol 194, Num 2, pp 508-511, issn 0002-9378, 4 p.Article

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosageLIAO, Jun; KOCHILAS, Lazaros; NOWOTSCHIN, Sonja et al.Human molecular genetics (Print). 2004, Vol 13, Num 15, pp 1577-1585, issn 0964-6906, 9 p.Article

Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndromeMARKERT, M. Louise; ALEXIEFF, Marilyn J; MAHAFFEY, Samuel M et al.Blood. 2004, Vol 104, Num 8, pp 2574-2581, issn 0006-4971, 8 p.Article

PRODH mutations and hyperprolinemia in a subset of schizophrenic patientsJACQUET, Hélène; RAUX, Grégory; BOU, Jacqueline et al.Human molecular genetics (Print). 2002, Vol 11, Num 19, pp 2243-2249, issn 0964-6906Article

Isolation of novel cDNA encompassing the ADU balanced translocation break point in the DiGeorge critical regionMYOUNG HEE KIM; HUR, Hyangsuk; PARK, Jonghoon et al.Molecular biotechnology. 2001, Vol 17, Num 3, pp 213-217, issn 1073-6085Article

Transcriptional regulation of cardiac development : Implications for congenital heart disease and DiGeorge syndromeEPSTEIN, Jonathan A; BUCK, Clayton A.Pediatric research. 2000, Vol 48, Num 6, pp 717-724, issn 0031-3998Article

An unusual concurrence of graft versus host disease caused by engraftment of maternal lymphocytes with DiGeorge anomalyOCEJO-VINYALS, J. G; LOZANO, M.-J; SANCHEZ-VELASCO, P et al.Archives of disease in childhood. 2000, Vol 83, Num 2, pp 165-169, issn 0003-9888Article

Transplantation of thymus tissue in complete DiGeorge syndromeMARKERT, M. L; BOECK, A; RICE, H. E et al.The New England journal of medicine. 1999, Vol 341, Num 16, pp 1180-1189, issn 0028-4793Article

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome)DIGILIO, M. C; PACIFICO, C; TIERI, L et al.British journal of audiology. 1999, Vol 33, Num 5, pp 329-334, issn 0300-5364Conference Paper