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Items: 1 to 20 of 104

1.

Pulmonary extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue associated with granulomatous inflammation in a child with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome).

Pongpruttipan T, Cook JR, Reyes-Mugica M, Spahr JE, Swerdlow SH.

J Pediatr. 2012 Nov;161(5):954-8. doi: 10.1016/j.jpeds.2012.07.003. Epub 2012 Aug 21.

2.

Epstein-Barr virus-positive T-cell lymphoma cells having chromosome 22q11.2 deletion: an autopsy report of DiGeorge syndrome.

Itoh S, Ohno T, Kakizaki S, Ichinohasama R.

Hum Pathol. 2011 Dec;42(12):2037-41. doi: 10.1016/j.humpath.2010.03.014. Epub 2011 Jun 17.

PMID:
21683977
3.

FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.

Yakut T, Kilic SS, Cil E, Yapici E, Egeli U.

Pediatr Surg Int. 2006 Apr;22(4):380-3. Epub 2006 Feb 4.

PMID:
16463032
4.

Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.

Staple L, Andrews T, McDonald-McGinn D, Zackai E, Sullivan KE.

Pediatr Allergy Immunol. 2005 May;16(3):226-30.

PMID:
15853951
5.

DiGeorge syndrome associated with solitary median maxillary central incisor.

Yang HC, Shyur SD, Huang LH, Chang YC, Wen DC, Liang PH, Lin MT.

Asian Pac J Allergy Immunol. 2005 Jun-Sep;23(2-3):159-63.

6.

Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.

Sullivan KE.

Immunol Allergy Clin North Am. 2008 May;28(2):353-66. doi: 10.1016/j.iac.2008.01.003. Review.

PMID:
18424337
7.

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

Kapadia RK, Bassett AS.

CMAJ. 2008 Feb 12;178(4):391-3. doi: 10.1503/cmaj.071300. No abstract available.

8.

Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.

Berend SA, Spikes AS, Kashork CD, Wu JM, Daw SC, Scambler PJ, Shaffer LG.

Am J Med Genet. 2000 Apr 10;91(4):313-7.

PMID:
10766989
9.

An adult case of 22q11.2 deletion syndrome diagnosed in a 36-year-old woman with hypocalcemia caused by hypoparathyroidism and Hashimoto's thyroiditis.

Nakada Y, Terui K, Kageyama K, Tsushima Y, Murakami H, Soma Y, Nigawara T, Sakihara S.

Intern Med. 2013;52(12):1365-8.

10.

A case of congenitally absent left internal carotid artery: vascular malformations in 22q11.2 deletion syndrome.

Johnson MD, Gentry LR, Rice GM, Mount DL.

Cleft Palate Craniofac J. 2010 May;47(3):314-7. doi: 10.5555/09-061.1.

PMID:
19860531
11.

[Genetic and clinical characteristics of 22q11.2 deletion syndrome].

Kozlova IuO, Zabnenkova VV, Shilova NV, Min'zhenkova ME, Antonenko VG, Kotlukova NP, Simonova LV, Kazanceva IA, Levchenko EG, Bombardirova TD, Zolotukhina TV, Poliakov AV.

Genetika. 2014 May;50(5):602-10. Russian.

PMID:
25715476
12.
13.

EBV-positive extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue in the posttransplant setting: a distinct type of posttransplant lymphoproliferative disorder?

Gibson SE, Swerdlow SH, Craig FE, Surti U, Cook JR, Nalesnik MA, Lowe C, Wood KM, Bacon CM.

Am J Surg Pathol. 2011 Jun;35(6):807-15. doi: 10.1097/PAS.0b013e3182190999.

PMID:
21552113
14.

A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.

Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.

Ophthalmic Genet. 2014 Dec;35(4):248-51. doi: 10.3109/13816810.2013.811269. Epub 2013 Jul 8.

PMID:
23834556
15.

Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion.

Van Hemel JO, Schaap C, Van Opstal D, Mulder MP, Niermeijer MF, Meijers JH.

J Med Genet. 1995 Aug;32(8):657-8.

16.

Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome).

Ysunza A, Pamplona MC, Ramírez E, Canún S, Sierra MC, Silva-Rojas A.

Int J Pediatr Otorhinolaryngol. 2003 Aug;67(8):911-5.

PMID:
12880672
17.

Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.

Shuib S, Abdul Latif Z, Abidin NZ, Akmal SN, Zakaria Z.

Malays J Pathol. 2009 Dec;31(2):133-6.

18.

DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.

Bartsch O, Nemecková M, Kocárek E, Wagner A, Puchmajerová A, Poppe M, Ounap K, Goetz P.

Am J Med Genet A. 2003 Feb 15;117A(1):1-5.

PMID:
12548732
19.

[Clinical features and molecular diagnosis of three patients with DiGeorge anomaly].

Sun JQ, Wang LS, Qi CH, Ying WJ, Guo XH, Liu DR, Hui XY, Liu F, Cao Y, Luo FH, Wang XC.

Zhonghua Er Ke Za Zhi. 2012 Dec;50(12):944-7. Chinese.

PMID:
23324155
20.

Anatomic patterns of conotruncal defects associated with deletion 22q11.

Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B.

Genet Med. 2001 Jan-Feb;3(1):45-8.

PMID:
11339377

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