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

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

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

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

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

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

Syndrome-Specific Growth Charts for 22q11.2 Deletion Syndrome in Caucasian ChildrenHABEL, Alex; MCGINN, Michael-John; ZACKAI, Elaine H et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 11, pp 2665-2671, issn 1552-4825, 7 p.Article

THE ASSOCIATION OF THE DIGEORGE ANOMALAD WITH PARTIAL MONOSOMY OF CHROMOSOME 22KELLEY RI; ZACKAI EH; EMANUEL BS et al.1982; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1982; VOL. 101; NO 2; PP. 197-200; BIBL. 22 REF.Article

Congenital Skin Pedicles With or Without Amniotic Band Sequence: Extending the Human Phenotype Resembling Mouse DisorganizationISIDOR, B; BAUJAT, G; LE CAIGNEC, C et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 8, pp 1734-1739, issn 1552-4825, 6 p.Article

Growth Charts for 22q11 Deletion SyndromeTARQUINIO, Daniel C; JONES, Marilyn C; LYONS JONES, Kenneth et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 11, pp 2672-2681, issn 1552-4825, 10 p.Article

The Role of Cephalometry in Assessing Velopharyngeal Dysfunction in Velocardiofacial SyndromeVEERAPANDIYAN, Aravindhan; BLALOCK, David; GHOSH, Srija et al.The Laryngoscope. 2011, Vol 121, Num 4, pp 732-737, issn 0023-852X, 6 p.Article

Ocular findings in children with a microdeletion in chromosome 22qll.2CASTEELS, Ingele; CASAER, Patricia; GEWILLIG, Marc et al.European journal of pediatrics. 2008, Vol 167, Num 7, pp 751-755, issn 0340-6199, 5 p.Article

Chromosome 22q11.2 Deletion Syndrome : DiGeorge Syndrome/ Velocardiofacial SyndromeSULLIVAN, Kathleen E.Immunology and allergy clinics of North America. 2008, Vol 28, Num 2, issn 0889-8561, ix, 353-366 [15 p.]Article

Distal 22qll.2 Microduplication Encompassing the BCR GeneDESCARTES, Maria; FRANKLIN, Judy; DIAZ DE STAHL, Teresita et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 23, pp 3075-3081, issn 1552-4825, 7 p.Article

A Patient With 22qll.2 Deletion and Opitz Syndrome-Like Phenotype Has the Same Deletion as Velocardiofacial PatientsERICKSON, Robert P; DIAZ DE STAHL, Teresita; BRUDER, Car E. G et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 24, pp 3302-3308, issn 1552-4825, 7 p.Article

Hippocampal Malrotation is Associated with Chromosome 22q11.2 MicrodeletionANDRADE, Danielle M; KRINGS, Timo; CHOW, Eva W. C et al.Canadian journal of neurological sciences. 2013, Vol 40, Num 5, pp 652-656, issn 0317-1671, 5 p.Article

Detection of Microdeletion 22q11.2 in a Fetus by Next-Generation Sequencing of Maternal PlasmaJENSEN, Taylor J; DZAKULA, Zeljko; DECIU, Cosmin et al.Clinical chemistry (Baltimore, Md.). 2012, Vol 58, Num 7, pp 1148-1151, issn 0009-9147, 4 p.Article

Aortic Root Dilation in Patients With 22q11.2 Deletion SyndromeJOHN, Anitha S; MCDONALD-MCGINN, Donna M; ZACKAI, Elaine H et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 5, pp 939-942, issn 1552-4825, 4 p.Article

Familial Exudative Vitreoretinopathy and DiGeorge Syndrome: A New Locus for Familial Exudative Vitreoretinopathy on Chromosome 22q11.2?GILMOUR, David F; DOWNEY, Louise M; SHERIDAN, Eamonn et al.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 8, pp 1522-1524, issn 0161-6420, 3 p.Article