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Items: 18

1.

An Adult Case of Chromosome 22q11.2 Deletion Syndrome Associated with a High-positioned Right Aortic Arch.

Hoshino Y, Machida M, Shimano SI, Taya T.

Intern Med. 2017;56(7):865-872. doi: 10.2169/internalmedicine.56.7558. Epub 2017 Apr 1.

2.

Synchronous Aberrant Cerebellar and Opercular Development in Fetuses and Neonates with Congenital Heart Disease: Correlation with Early Communicative Neurodevelopmental Outcomes, Initial Experience.

Wong A, Chavez T, O'Neil S, Votava-Smith J, Miller D, delCastillo S, Panigrahy A, Paquette L.

AJP Rep. 2017 Jan;7(1):e17-e27. doi: 10.1055/s-0036-1597934.

3.

Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts.

Yi JJ, Weinberger R, Moore TM, Calkins ME, Guri Y, McDonald-McGinn DM, Zackai EH, Emanuel BS, Gur RE, Gothelf D, Gur RC.

Brain Cogn. 2016 Jul;106:33-41. doi: 10.1016/j.bandc.2016.02.002. Epub 2016 May 17.

4.

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia.

Forstner AJ, Basmanav FB, Mattheisen M, Böhmer AC, Hollegaard MV, Janson E, Strengman E, Priebe L, Degenhardt F, Hoffmann P, Herms S, Maier W, Mössner R, Rujescu D, Ophoff RA, Moebus S, Mortensen PB, Børglum AD, Hougaard DM, Frank J, Witt SH, Rietschel M, Zimmer A, Nöthen MM, Miró X, Cichon S.

J Psychiatry Neurosci. 2014 Nov;39(6):386-96.

5.

Cortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: a longitudinal study.

Kunwar A, Ramanathan S, Nelson J, Antshel KM, Fremont W, Higgins AM, Shprintzen RJ, Kates WR.

Schizophr Res. 2012 May;137(1-3):20-5. doi: 10.1016/j.schres.2012.01.032. Epub 2012 Feb 22.

6.

Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Eisenberg DP, Jabbi M, Berman KF.

Neuroimage. 2010 Nov 15;53(3):857-69. doi: 10.1016/j.neuroimage.2010.02.070. Epub 2010 Mar 3. Review.

7.

The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome.

Zaleski C, Bassett AS, Tam K, Shugar AL, Chow EW, McPherson E.

Am J Med Genet A. 2009 Mar;149A(3):525-8. doi: 10.1002/ajmg.a.32650. No abstract available.

8.

Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome.

Chow EW, Zipursky RB, Mikulis DJ, Bassett AS.

Biol Psychiatry. 2002 Feb 1;51(3):208-15.

9.

Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia.

Chow EW, Mikulis DJ, Zipursky RB, Scutt LE, Weksberg R, Bassett AS.

Biol Psychiatry. 1999 Nov 15;46(10):1436-42.

10.

22q11 deletion syndrome: a genetic subtype of schizophrenia.

Bassett AS, Chow EW.

Biol Psychiatry. 1999 Oct 1;46(7):882-91. Review.

11.

Phenotype of adults with the 22q11 deletion syndrome: A review.

Cohen E, Chow EW, Weksberg R, Bassett AS.

Am J Med Genet. 1999 Oct 8;86(4):359-65. Review.

12.

22q11 deletion syndrome in adults with schizophrenia.

Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R.

Am J Med Genet. 1998 Jul 10;81(4):328-37.

13.

Absence of a del(22q11) in a patient with the 3C (craniocerebellocardiac) syndrome.

Saraiva JM, Matoso E, Marques I.

J Med Genet. 1998 Apr;35(4):347-8. No abstract available.

14.

Velocardiofacial syndrome.

Pike AC, Super M.

Postgrad Med J. 1997 Dec;73(866):771-5. Review.

15.

Radial aplasia and chromosome 22q11 deletion.

Digilio MC, Giannotti A, Marino B, Guadagni AM, Orzalesi M, Dallapiccola B.

J Med Genet. 1997 Nov;34(11):942-4.

16.

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Ryan AK, Goodship JA, Wilson DI, Philip N, Levy A, Seidel H, Schuffenhauer S, Oechsler H, Belohradsky B, Prieur M, Aurias A, Raymond FL, Clayton-Smith J, Hatchwell E, McKeown C, Beemer FA, Dallapiccola B, Novelli G, Hurst JA, Ignatius J, Green AJ, Winter RM, Brueton L, Brøndum-Nielsen K, Scambler PJ, et al.

J Med Genet. 1997 Oct;34(10):798-804.

17.
18.

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.

Hatchwell E.

J Med Genet. 1996 Mar;33(3):261. No abstract available.

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