DiGeorge Anomaly in the Absence of Chromosome 22p11.2 DeletionROPE, Alan F; CRAGUN, Deborah L; SAAL, Howard M et al.The Journal of pediatrics. 2009, Vol 155, Num 4, pp 560-565, issn 0022-3476, 6 p.Article

Vertebral Defects as an Unusual Mode of Presentation of 22q11.2 DeletionFAIVRE, L; MASUREL-PAULET, A; CALLIER, P et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 12, pp 2865-2866, issn 1552-4825, 2 p.Article

22q11.2 deletion carriers and schizophrenia-associated novel variantsBALAN, S; IWAYAMA, Y; TOYOTA, T et al.British journal of psychiatry (Print). 2014, Vol 204, Num 5, pp 398-399, issn 0007-1250, 2 p.Article

Immunoglobulin Deficiencies: The B-Lymphocyte Side of DiGeorge SyndromePATEL, Kiran; AKHTER, Javeed; KOBRYNSKI, Lisa et al.The Journal of pediatrics. 2012, Vol 161, Num 5, pp 950-953, issn 0022-3476, 4 p.Article

Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in spermMAOQING TONG; KATO, Takema; YAMADA, Kouji et al.Human molecular genetics (Print). 2010, Vol 19, Num 13, pp 2630-2637, issn 0964-6906, 8 p.Article

MOZ Regulates the Tbx1 Locus, and Moz Mutation Partially Phenocopies DiGeorge SyndromeVOSS, Anne K; VANYAI, Hannah K; COLLIN, Caitlin et al.Developmental cell. 2012, Vol 23, Num 3, pp 652-663, issn 1534-5807, 12 p.Article

Social cognition in 22q11.2 microdeletion syndrome: Relevance to psychosis?JALBRZIKOWSKI, Maria; CARTER, Chelsea; SENTURK, Damla et al.Schizophrenia research. 2012, Vol 142, Num 1-3, pp 99-107, issn 0920-9964, 9 p.Article

Isolated Innominate Artery From the Main Pulmonary Artery in DiGeorge SyndromeKREEGER, Joe; SCHLOSSER, Brian; SALLEE, Denver et al.Journal of the American College of Cardiology. 2011, Vol 57, Num 6, issn 0735-1097, p. 753Article

Developmental perspectives on copy number abnormalities of the 22q11.2 regionTAN, T. Y; GORDON, C. T; AMOR, D. J et al.Clinical genetics. 2010, Vol 78, Num 3, pp 201-218, issn 0009-9163, 18 p.Article

Thymus transplantationMARKERT, M. Louise; DEVLIN, Blythe H; MCCARTHY, Elizabeth A et al.Clinical immunology (Orlando, Fla. Print). 2010, Vol 135, Num 2, pp 236-246, issn 1521-6616, 11 p.Article

The cutaneous manifestations of atypical complete DiGeorge syndrome : a histopathologic and immunohistochemical studyANGELICA SELIM, Maria; MARKERT, Mary L; BURCHETTE, James L et al.Journal of cutaneous pathology. 2008, Vol 35, Num 4, pp 380-385, issn 0303-6987, 6 p.Article

Factors Affecting Success of Thymus Transplantation for Complete DiGeorge AnomalyMARKERT, M. L; DEVLIN, B. H; CHINN, I. K et al.American journal of transplantation (Print). 2008, Vol 8, Num 8, pp 1729-1736, issn 1600-6135, 8 p.Article

Additional Case of an Uncommon 22q11.2 Reciprocal Rearrangement in a Phenotypically Normal Mother of Children With 22q11.2 Deletion and 22q11.2 Duplication SyndromesFERNANDEZ, Luis; NEVADO, Julián; LAPUNZINA, Pablo et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 11, pp 2963-2968, issn 1552-4825, 6 p.Article

Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo eventsWEIMIN BI; PROBST, Frank J; LUPSKI, James R et al.Journal of medical genetics. 2012, Vol 49, Num 11, pp 681-688, issn 0022-2593, 8 p.Article

Congenital Heart Defects in a Novel Recurrent 22q11.2 Deletion Harboring the Genes CRKL and MAPK.1BRECKPOT, Jeroen; THIENPONT, Bernard; BAUTERS, Marijke et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 3, pp 574-580, issn 1552-4825, 7 p.Article

Multicenter survey on the outcome of transplantation of hematopoietic cells in patients with the complete form of DiGeorge anomalyJANDA, Ales; SEDLACEK, Petr; BORDIGONI, Pierre et al.Blood. 2010, Vol 116, Num 13, pp 2229-2236, issn 0006-4971, 8 p.Article

The UFD1L rs5992403 polymorphism is associated with age at onset of schizophreniaKIYOMI OTA, Vanessa; IOLE BELANGERO, Sintia; ISABEL MELARAGNO, Maria et al.Journal of psychiatric research. 2010, Vol 44, Num 15, pp 1113-1115, issn 0022-3956, 3 p.Article

Immune constitution monitoring after PBMC transplantation in complete DiGeorge syndrome : An eight-year follow-upDAGUINDAU, Nicolas; DECOT, Véronique; BORDIGONI, Pierre et al.Clinical immunology (Orlando, Fla. Print). 2008, Vol 128, Num 2, pp 164-171, issn 1521-6616, 8 p.Article

Extracardiac features predicting 22qll.2 Deletion Syndrome in adult congenital heart diseaseFUNG, Wai Lun Alan; CHOW, Eva W. C; WEBB, Gary D et al.International journal of cardiology. 2008, Vol 131, Num 1, pp 51-58, issn 0167-5273, 8 p.Article

Role of SNAP29, LZTR1 and P2RXL1 genes on immune regulation in a patient with atypical 0.5 Mb deletion in 22q11.2 regionDE QUEIROZ SOARES, Diogo Cordeiro; LETIS DUTRA, Roberta; D'ANGIOLI COSTA QUAIO, Caio Robledo et al.Clinical immunology (Orlando, Fla. Print). 2012, Vol 145, Num 1, pp 55-58, issn 1521-6616, 4 p.Article

Phenotypic Variability of Atypical 22q11.2 Deletions Not Including TBX1VERHAGEN, Judith M. A; DIDERICH, Karin E. M; SREBNIAK, Malgorzata I et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2412-2420, issn 1552-4825, 9 p.Article

Evidence for Involvement of GNB1L in AutismCHEN, Ying-Zhang; MATSUSHITA, Mark; SHELLENBERG, Gerard D et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2012, Vol 159, Num 1, pp 61-71, issn 1552-4841, 11 p.Article

Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletionsCOSTAIN, Gregory; CHOW, Eva W. C; SILVERSIDES, Candice K et al.Journal of medical genetics. 2011, Vol 48, Num 12, pp 819-824, issn 0022-2593, 6 p.Article

Safety and efficacy of measles, mumps, and rubella vaccine in patients with DiGeorge syndromeAL-SUKAITI, Nashat; REID, Brenda; LAVI, Sasson et al.Journal of allergy and clinical immunology. 2010, Vol 126, Num 4, pp 868-869, issn 0091-6749, 2 p.Article

Unrelated Chromosomal Anomalies Found in Patients With Suspected 22qll.2 DeletionFEMANDEZ, Luis; LAPUNZINA, Pablo; GALAN-GOMEZ, Enrique et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 9, pp 1134-1141, issn 1552-4825, 8 p.Article