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    Results: 1 to 20 of 1483

    1.

    Double Aortic Arch with Dominant Left Arch and Right Ligamentum Arteriosum.

    Hashmi SF, Hanif M, Maroo S, Pollock J.

    Congenit Heart Dis. 2009 Nov;4(6):474-477.PMID: 19925543 [PubMed - as supplied by publisher]Related articles

    2.

    Isolated congenital heart disease is associated with the 22q11 deletion even though it is rare.

    Jiang L, Hou Z, Duan C, Chen B, Chen Z, Li Y, Huan Y, Wu KK.

    Int J Cardiol. 2009 Nov 16. [Epub ahead of print]PMID: 19923022 [PubMed - as supplied by publisher]Related articles

    3.

    The male-determining gene SRY is a hybrid of DGCR8 and SOX3, and is regulated by the transcription factor CP2.

    Sato Y, Shinka T, Sakamoto K, Ewis AA, Nakahori Y.

    Mol Cell Biochem. 2009 Nov 10. [Epub ahead of print]PMID: 19902333 [PubMed - as supplied by publisher]Related articles

    4.

    Effect of a syndromic diagnosis on mandibular size and sagittal position in Robin sequence.

    Rogers G, Lim AA, Mulliken JB, Padwa BL.

    J Oral Maxillofac Surg. 2009 Nov;67(11):2323-31.PMID: 19837298 [PubMed - indexed for MEDLINE]Related articles

    5.

    Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome).

    Tan GM, Arnone D, McIntosh AM, Ebmeier KP.

    Schizophr Res. 2009 Dec;115(2-3):173-81. Epub 2009 Oct 9.PMID: 19819113 [PubMed - in process]Related articles

    6.

    Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.

    Meechan DW, Tucker ES, Maynard TM, LaMantia AS.

    Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16434-45. Epub 2009 Sep 10.PMID: 19805316 [PubMed - indexed for MEDLINE]Related articles

    7.

    Tbx1 regulates proliferation and differentiation of multipotent heart progenitors.

    Chen L, Fulcoli FG, Tang S, Baldini A.

    Circ Res. 2009 Oct 23;105(9):842-51. Epub 2009 Sep 10.PMID: 19745164 [PubMed - indexed for MEDLINE]Related articles

    8.

    Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm.

    Calmont A, Ivins S, Van Bueren KL, Papangeli I, Kyriakopoulou V, Andrews WD, Martin JF, Moon AM, Illingworth EA, Basson MA, Scambler PJ.

    Development. 2009 Sep;136(18):3173-83.PMID: 19700621 [PubMed - indexed for MEDLINE]Related articles

    9.

    Fish based preimplantation genetic diagnosis to prevent DiGeorge syndrome.

    Shefi S, Raviv G, Rienstein S, Barkai G, Aviram-Goldring A, Levron J.

    J Assist Reprod Genet. 2009 Jul;26(7):411-3. Epub 2009 Aug 13.PMID: 19680801 [PubMed - in process]Related articles

    10.

    Seizures and EEG findings in an adult patient with DiGeorge syndrome: a case report and review of the literature.

    González W, Bautista RE.

    Seizure. 2009 Nov;18(9):648-51. Epub 2009 Aug 7.PMID: 19665396 [PubMed - in process]Related articles

    11.

    Truncal valve repair in neonates using pericardial leaflet extension.

    Bahrami S, Mitropoulos F, Leong F, Levi DS, Laks H, Plunkett MD.

    Congenit Heart Dis. 2009 Jul;4(4):281-3.PMID: 19664033 [PubMed - indexed for MEDLINE]Related articles

    12.

    Understanding cleft lip and palate. 1: an overview.

    Slator R, Russell J, Bridges M, Tomlinson J, Cole A, Morton J.

    J Fam Health Care. 2009;19(3):101-3.PMID: 19645155 [PubMed - indexed for MEDLINE]Related articles

    13.

    Velopharyngoplasty for noncleft velopharyngeal insufficiency: results in relation to 22q11 microdeletion.

    Rouillon I, Leboulanger N, Roger G, Maulet M, Marlin S, Loundon N, Portnoï MF, Denoyelle F, Garabédian EN.

    Arch Otolaryngol Head Neck Surg. 2009 Jul;135(7):652-6.PMID: 19620585 [PubMed - indexed for MEDLINE]Related articles

    14.

    DiGeorge anomaly in the absence of chromosome 22q11.2 deletion.

    Rope AF, Cragun DL, Saal HM, Hopkin RJ.

    J Pediatr. 2009 Oct;155(4):560-5.PMID: 19595366 [PubMed - indexed for MEDLINE]Related articles

    15.

    THE USE OF COMPARATIVE GENOMIC HYBRIDIZATION AND FLUORESCENT IN SITU HYBRIDIZATION IN POSTMORTEM PATHOLOGY INVESTIGATION OF CONGENITAL MALFORMATIONS.

    Goemaere N, Douben H, van Opstal D, Wouters C, Tibboel D, De Krijger RR, de Klein A.

    Pediatr Dev Pathol. 2009 Jul 13:1. [Epub ahead of print]PMID: 19594201 [PubMed - as supplied by publisher]Related articles

    16.

    Focal adhesion kinase is required for neural crest cell morphogenesis during mouse cardiovascular development.

    Vallejo-Illarramendi A, Zang K, Reichardt LF.

    J Clin Invest. 2009 Aug;119(8):2218-30. doi: 10.1172/JCI38194. Epub 2009 Jul 1.PMID: 19587446 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Tbx1 regulates the BMP-Smad1 pathway in a transcription independent manner.

    Fulcoli FG, Huynh T, Scambler PJ, Baldini A.

    PLoS One. 2009 Jun 25;4(6):e6049.PMID: 19557177 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    [Evaluation of the efficiency of ERTL4/6 screening tests for language disorders for children with a 22q11 deletion]

    Deggouj N, Estienne F, Derue L, Vanderlinden F, Ovaert C, Sluysmans T, Gersdorff M.

    Rev Laryngol Otol Rhinol (Bord). 2009;130(1):41-4. French. PMID: 19530523 [PubMed - indexed for MEDLINE]Related articles

    19.

    Unusual four-generation chromosome-22 rearrangement: when "normality" masks abnormality.

    Nevado J, de Torres ML, Fernández L, Mori MA, Villa A, Palomares M, García-Santiago F, Mansilla E, García-Miñaur S, Delicado A, Lapunzina P.

    Am J Med Genet A. 2009 Jul;149A(7):1561-4. No abstract available. PMID: 19530191 [PubMed - indexed for MEDLINE]Related articles

    20.

    The dynamics of T-cell receptor repertoire diversity following thymus transplantation for DiGeorge anomaly.

    Ciupe SM, Devlin BH, Markert ML, Kepler TB.

    PLoS Comput Biol. 2009 Jun;5(6):e1000396. Epub 2009 Jun 12.PMID: 19521511 [PubMed - indexed for MEDLINE]Related articlesFree article

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