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Oral findings if DiGeorge syndromeJENSEN, S. B; JACOBSEN, P; ROTNE, L et al.International journal of oral surgery. 1983, Vol 12, Num 4, pp 250-254, issn 0300-9785Article

LE SYNDROME DE DIGEORGE. A PROPOS DE DEUX OBSERVATIONSPALMIER ARMELLE.sd; FRA; DA. S.D.; 137; PAGINATION MULT.-1 PL.: ILL.; 30 CM; BIBL. 119 REF.; TH.: MED./MONTPELLIER/1979Thesis

LE SYNDROME DE DI GEORGE: A PROPOS DE DEUX OBSERVATIONSBERNARD R; ELBAZE F; FIESCHI JB et al.1980; PEDIATRIE; ISSN 0031-4021; FRA; DA. 1980; VOL. 35; NO 7; PP. 611-617; BIBL. 24 REF.Article

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Live viral vaccines in patients with partial DiGeorge syndrome: clinical experience and cellular immunityMOYLETT, Edina H; WASAN, Anita N; NOROSKI, Lenora M et al.Clinical immunology (Orlando, Fla. Print). 2004, Vol 112, Num 1, pp 106-112, issn 1521-6616, 7 p.Article

THE SPECTRUM OF THE DI GEORGE SYNDROMECONLEY ME; BLECKWITH JB; MANCER JFK et al.1979; J. PEDIATR.; USA; DA. 1979; VOL. 94; NO 6; PP. 883-890; BIBL. 41 REF.Article

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THE ORIGIN OF HUMAN NK CELLS AN ONTOGENIC MODEL DERIVED FROM STUDIES IN PATIENTS WITH IMMUNODEFICIENCIESPETER HH.1983; BLUT; ISSN 0006-5242; DEU; DA. 1983; VOL. 46; NO 5; PP. 239-248; BIBL. 3 P.Article

UNTERSUCHUNGEN ZUM EINFLUSS VON SUBSTANZ P UND TEILSEQUENZEN DER VERBINDUNG AUF DIE ANGIOTENSIN I-CONVERTING-ENZYM-AKTIVITAET = RECHERCHES SUR L'INFLUENCE DE LA SUBSTANCE P ET LES SEQUENCES PARTIELLES DE CE COMPOSE SUR L'ACTIVITE DE L'ENZYME CONVERTISSANT L'ANGIOTENSINE ISIEMS WE; KOMISSAROWA NW; GOMASKOW OA et al.1983; PHARMAZIE; ISSN 0031-7144; DDR; DA. 1983; VOL. 38; NO 4; PP. 256-257; ABS. ENG; BIBL. 11 REF.Article

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

Síndrome de digeorge asociado a hemimelia = Di george syndrome associated with hemimeliaVERA DE PEDRO, E; SALADO MARIN, C; BOTELLA ASTORQUI, M et al.Anales de pediatria (2003. Ed. impresa). 2007, Vol 66, Num 6, pp 628-630, issn 1695-4033, 3 p.Article

Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?VITELLI, Francesca; BALDINI, Antonio.Trends in genetics (Regular ed.). 2003, Vol 19, Num 11, pp 588-593, issn 0168-9525, 6 p.Article

Neurocognitive profile in 22q11 deletion syndrome and schizophreniaCHOW, Eva W. C; WATSON, Mark; YOUNG, Donald A et al.Schizophrenia research. 2006, Vol 87, Num 1-3, pp 270-278, issn 0920-9964, 9 p.Article

Complete DiGeorge syndrome: Development of rash, lymphadenopathy, and oligoclonal T cells in 5 casesMARKERT, M. Louise; ALEXIEFF, Marilyn J; BUCKLEY, Rebecca H et al.Journal of allergy and clinical immunology. 2004, Vol 113, Num 4, pp 734-741, issn 0091-6749, 8 p.Article

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

Presenting phenotype in 100 children with the 22q11 deletion syndromeOSKARSDOTTIR, Solveig; PERSSON, Christina; ERIKSSON, Bengt O et al.European journal of pediatrics. 2005, Vol 164, Num 3, pp 146-153, issn 0340-6199, 8 p.Article

Humoral immune responses and CD27 + B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome)FINOCCHI, A; DI CESARE, S; ROMITI, M. L et al.Pediatric allergy and immunology. 2006, Vol 17, Num 5, pp 382-388, issn 0905-6157, 7 p.Article

Anesthetic management of a child with chromosome 22q11 deletion syndromeYOTSUI-TSUCHIMOCHI, Hiroe; HIGA, Kazuo; MATSUNAGA, Matsuko et al.Paediatric anaesthesia (Paris). 2006, Vol 16, Num 4, pp 454-457, issn 1155-5645, 4 p.Article

Maturational alterations of peripheral T cell subsets and cytokine gene expression in 22q11.2 deletion syndromeKANAYA, Y; OHGA, S; IKEDA, K et al.Clinical and experimental immunology (Print). 2006, Vol 144, Num 1, pp 85-93, issn 0009-9104, 9 p.Article

Long-term assessment of T-cell populations in DiGeorge syndromeCHINEN, Javier; ROSENBLATT, Howard M; O'BRIAN SMITH, E et al.Journal of allergy and clinical immunology. 2003, Vol 111, Num 3, pp 573-579, issn 0091-6749, 7 p.Article

Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of digeorge/velocardiofacial syndromeBRUNET, Anna; GABAU, Elisabeth; PERICH, Rosa Maria et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 22, pp 2426-2432, issn 1552-4825, 7 p.Article

Selective IgM deficiency and 22q11.2 deletion syndromeKUNG, Shiang-Ju; GRIPP, Karen W; STEPHAN, Mark J et al.Annals of allergy, asthma, & immunology. 2007, Vol 99, Num 1, pp 87-92, issn 1081-1206, 6 p.Article

Antenatal diagnosis of DiGeorge syndromeDRISCOLL, D. A; BUDARF, M. L; EMANUEL, B. S et al.Lancet (British edition). 1991, Vol 338, Num 8779, pp 1390-1391, issn 0140-6736Article

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