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Items: 1 to 20 of 29

1.

Aortic, Right Arches.

Law MA, Bhimji SS.

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2017 Jun-.
2017 May 22.

2.

The importance of understanding cognitive trajectories: the case of 22q11.2 deletion syndrome.

Swillen A.

Curr Opin Psychiatry. 2016 Mar;29(2):133-7. doi: 10.1097/YCO.0000000000000231. Review.

3.

Fetuses with right aortic arch: a multicenter cohort study and meta-analysis.

D'Antonio F, Khalil A, Zidere V, Carvalho JS.

Ultrasound Obstet Gynecol. 2016 Apr;47(4):423-32. doi: 10.1002/uog.15805. Epub 2016 Mar 16. Review.

4.

Hard to swallow: Developmental biological insights into pediatric dysphagia.

LaMantia AS, Moody SA, Maynard TM, Karpinski BA, Zohn IE, Mendelowitz D, Lee NH, Popratiloff A.

Dev Biol. 2016 Jan 15;409(2):329-42. doi: 10.1016/j.ydbio.2015.09.024. Epub 2015 Nov 7. Review.

5.

Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome.

Tang KL, Antshel KM, Fremont WP, Kates WR.

J Dev Behav Pediatr. 2015 Oct;36(8):639-50. doi: 10.1097/DBP.0000000000000210. Review.

6.

22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features.

Burnside RD.

Cytogenet Genome Res. 2015;146(2):89-99. doi: 10.1159/000438708. Epub 2015 Aug 8. Review.

7.

22q11 deletion syndrome: current perspective.

Hacıhamdioğlu B, Hacıhamdioğlu D, Delil K.

Appl Clin Genet. 2015 May 18;8:123-32. doi: 10.2147/TACG.S82105. eCollection 2015. Review.

8.

Developmental trajectories in 22q11.2 deletion.

Swillen A, McDonald-McGinn D.

Am J Med Genet C Semin Med Genet. 2015 Jun;169(2):172-81. doi: 10.1002/ajmg.c.31435. Epub 2015 May 18. Review.

9.

History and current status of newborn screening for severe combined immunodeficiency.

Kwan A, Puck JM.

Semin Perinatol. 2015 Apr;39(3):194-205. doi: 10.1053/j.semperi.2015.03.004. Epub 2015 Apr 30. Review.

10.

Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.

Grande M, Jansen FA, Blumenfeld YJ, Fisher A, Odibo AO, Haak MC, Borrell A.

Ultrasound Obstet Gynecol. 2015 Dec;46(6):650-8. doi: 10.1002/uog.14880. Review.

11.

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Meechan DW, Maynard TM, Tucker ES, Fernandez A, Karpinski BA, Rothblat LA, LaMantia AS.

Prog Neurobiol. 2015 Jul;130:1-28. doi: 10.1016/j.pneurobio.2015.03.004. Epub 2015 Apr 9. Review.

12.

CHARGE syndrome: a review of the immunological aspects.

Wong MT, Schölvinck EH, Lambeck AJ, van Ravenswaaij-Arts CM.

Eur J Hum Genet. 2015 Nov;23(11):1451-9. doi: 10.1038/ejhg.2015.7. Epub 2015 Feb 18. Review.

13.

Keratoconus in an adult with 22q11.2 deletion syndrome.

Saffra N, Reinherz B.

BMJ Case Rep. 2015 Jan 16;2015. pii: bcr2014203737. doi: 10.1136/bcr-2014-203737. Review.

14.

Practical guidelines for managing adults with 22q11.2 deletion syndrome.

Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, Silversides C, Swillen A, van Amelsvoort T, McDonald-McGinn DM, Bassett AS.

Genet Med. 2015 Aug;17(8):599-609. doi: 10.1038/gim.2014.175. Epub 2015 Jan 8. Review.

15.

22q11.2 deletion syndrome.

McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS.

Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Review.

16.

miRNA biogenesis: biological impact in the development of cancer.

Romero-Cordoba SL, Salido-Guadarrama I, Rodriguez-Dorantes M, Hidalgo-Miranda A.

Cancer Biol Ther. 2014;15(11):1444-55. doi: 10.4161/15384047.2014.955442. Review.

17.

Evolutionary and developmental origins of the cardiac neural crest: building a divided outflow tract.

Keyte AL, Alonzo-Johnsen M, Hutson MR.

Birth Defects Res C Embryo Today. 2014 Sep;102(3):309-23. doi: 10.1002/bdrc.21076. Epub 2014 Sep 16. Review.

18.

'Black sheep' that don't leave the double-stranded RNA-binding domain fold.

Gleghorn ML, Maquat LE.

Trends Biochem Sci. 2014 Jul;39(7):328-40. doi: 10.1016/j.tibs.2014.05.003. Epub 2014 Jun 19. Review.

19.

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, Vorstman J, Duijff SN, Klaassen PW, Swillen A, Gothelf D, Green T, Weizman A, Van Amelsvoort T, Evers L, Boot E, Shashi V, Hooper SR, Bearden CE, Jalbrzikowski M, Armando M, Vicari S, Murphy DG, Ousley O, Campbell LE, Simon TJ, Eliez S; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Am J Psychiatry. 2014 Jun;171(6):627-39. Review.

20.

MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review.

Forstner AJ, Degenhardt F, Schratt G, Nöthen MM.

Front Mol Neurosci. 2013 Dec 5;6:47. doi: 10.3389/fnmol.2013.00047. Review.

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