Similar articles for PMID: 18268261

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1

Recognizing a common genetic syndrome: 22q11.2 deletion syndrome.

Kapadia RK, Bassett AS. Kapadia RK, et al. CMAJ. 2008 Feb 12;178(4):391-3. doi: 10.1503/cmaj.071300. CMAJ. 2008. PMID: 18268261 Free PMC article. No abstract available.

2

[Diagnosis of 22q11.2 deletion syndrome in the context of newly developed psychosis].

Kaltenboeck A, Friedrich F, Hinterbuchinger B, Litvan Z, Mossaheb N. Kaltenboeck A, et al. Neuropsychiatr. 2016 Dec;30(4):223-226. doi: 10.1007/s40211-016-0203-0. Epub 2016 Nov 7. Neuropsychiatr. 2016. PMID: 27822729 German.

3

[Prenatal diagnosis of 22q11 microdeletion syndrome].

Cai M, Huang H, Lin N, Guo N, Wu X, Su L, Xu L. Cai M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):192-195. doi: 10.3760/cma.j.issn.1003-9406.2017.02.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397216 Chinese.

4

Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

McDonald-McGinn DM, Reilly A, Wallgren-Pettersson C, Hoyme HE, Yang SP, Adam MP, Zackai EH, Sullivan KE. McDonald-McGinn DM, et al. Am J Med Genet A. 2006 Apr 15;140(8):906-9. doi: 10.1002/ajmg.a.31199. Am J Med Genet A. 2006. PMID: 16532473 Review. No abstract available.

5

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

Bassett AS, McDonald-McGinn DM, Devriendt K, Digilio MC, Goldenberg P, Habel A, Marino B, Oskarsdottir S, Philip N, Sullivan K, Swillen A, Vorstman J; International 22q11.2 Deletion Syndrome Consortium. Bassett AS, et al. J Pediatr. 2011 Aug;159(2):332-9.e1. doi: 10.1016/j.jpeds.2011.02.039. Epub 2011 May 12. J Pediatr. 2011. PMID: 21570089 Free PMC article. No abstract available.

6

Counseling families with chromosome 22q11 deletions: the catch in CATCH-22.

Bristow JD, Bernstein HS. Bristow JD, et al. J Am Coll Cardiol. 1998 Aug;32(2):499-501. doi: 10.1016/s0735-1097(98)00273-3. J Am Coll Cardiol. 1998. PMID: 9708482 Free article. No abstract available.

7

Preimplantation genetic diagnosis of DiGeorge syndrome.

Iwarsson E, Ahrlund-Richter L, Inzunza J, Fridström M, Rosenlund B, Hillensjö T, Sjöblom P, Nordenskjöld M, Blennow E. Iwarsson E, et al. Mol Hum Reprod. 1998 Sep;4(9):871-5. doi: 10.1093/molehr/4.9.871. Mol Hum Reprod. 1998. PMID: 9783847

8

Prenatal diagnosis of the 22q11.2 deletion syndrome.

Driscoll DA. Driscoll DA. Genet Med. 2001 Jan-Feb;3(1):14-8. doi: 10.1097/00125817-200101000-00004. Genet Med. 2001. PMID: 11339370 Free article. Review.

9

A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.

Erickson RP, Díaz de Ståhl T, Bruder CE, Dumanski JP. Erickson RP, et al. Am J Med Genet A. 2007 Dec 15;143A(24):3302-8. doi: 10.1002/ajmg.a.32025. Am J Med Genet A. 2007. PMID: 18000907

10

Introduction: advances in research on velo-cardio-facial syndrome/22q11.2 deletion syndrome.

Kates WR, Emanuel BS. Kates WR, et al. Dev Disabil Res Rev. 2008;14(1):1-2. doi: 10.1002/ddrr.1. Dev Disabil Res Rev. 2008. PMID: 18636630 No abstract available.

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