122 related articles for article (PubMed ID: 2063928)
1. DiGeorge anomaly associated with 10p deletion.
Monaco G; Pignata C; Rossi E; Mascellaro O; Cocozza S; Ciccimarra F
Am J Med Genet; 1991 May; 39(2):215-6. PubMed ID: 2063928
[TBL] [Abstract][Full Text] [Related]
2. DiGeorge anomaly and chromosome 10p deletions: one or two loci?
Dasouki M; Jurecic V; Phillips JA; Whitlock JA; Baldini A
Am J Med Genet; 1997 Nov; 73(1):72-5. PubMed ID: 9375926
[TBL] [Abstract][Full Text] [Related]
3. The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.
Van Esch H; Groenen P; Fryns JP; Van de Ven W; Devriendt K
Genet Couns; 1999; 10(1):59-65. PubMed ID: 10191430
[TBL] [Abstract][Full Text] [Related]
4. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
Matsuoka R; Takao A; Kimura M; Imamura S; Kondo C; Joh-o K; Ikeda K; Nishibatake M; Ando M; Momma K
Am J Med Genet; 1994 Nov; 53(3):285-9. PubMed ID: 7856665
[TBL] [Abstract][Full Text] [Related]
5. DiGeorge syndrome and partial monosomy 10p: case report and review.
Schuffenhauer S; Seidel H; Oechsler H; Belohradsky B; Bernsau U; Murken J; Meitinger T
Ann Genet; 1995; 38(3):162-7. PubMed ID: 8540688
[TBL] [Abstract][Full Text] [Related]
6. Deletion of the short arm of chromosome 10 (10p13): report of a patient and review.
Shapira M; Borochowitz Z; Bar-El H; Dar H; Etzioni A; Lorber A
Am J Med Genet; 1994 Aug; 52(1):34-8. PubMed ID: 7977458
[TBL] [Abstract][Full Text] [Related]
7. 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; 91(4):313-7. PubMed ID: 10766989
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 19595366
[TBL] [Abstract][Full Text] [Related]
9. The DiGeorge anomaly (CATCH 22, DiGeorge/velocardiofacial syndrome).
Hong R
Semin Hematol; 1998 Oct; 35(4):282-90. PubMed ID: 9801257
[TBL] [Abstract][Full Text] [Related]
10. Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome.
Yatsenko SA; Yatsenko AN; Szigeti K; Craigen WJ; Stankiewicz P; Cheung SW; Lupski JR
Clin Genet; 2004 Aug; 66(2):128-36. PubMed ID: 15253763
[TBL] [Abstract][Full Text] [Related]
11. Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literature.
Dallapiccola B; Marino B; Giannotti A; Valorani G
Ann Genet; 1989; 32(2):92-6. PubMed ID: 2667458
[TBL] [Abstract][Full Text] [Related]
12. Submicroscopic deletions at 22q11.2: variability of the clinical picture and delineation of a commonly deleted region.
Lindsay EA; Greenberg F; Shaffer LG; Shapira SK; Scambler PJ; Baldini A
Am J Med Genet; 1995 Mar; 56(2):191-7. PubMed ID: 7625444
[TBL] [Abstract][Full Text] [Related]
13. A common region of 10p deleted in DiGeorge and velocardiofacial syndromes.
Daw SC; Taylor C; Kraman M; Call K; Mao J; Schuffenhauer S; Meitinger T; Lipson T; Goodship J; Scambler P
Nat Genet; 1996 Aug; 13(4):458-60. PubMed ID: 8696341
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly.
Greenberg F; Courtney KB; Wessels RA; Huhta J; Carpenter RJ; Rich DC; Ledbetter DH
Am J Med Genet; 1988 Sep; 31(1):1-4. PubMed ID: 3066218
[TBL] [Abstract][Full Text] [Related]
15. [Monosomy 22pter-22q11.2 with monosomy 10q26.2-10qter without Di George syndrome].
Arslanian A; Veneziano G; Grasso M; Brugo A; Bertamino F
Pathologica; 1985; 77(1052):767-70. PubMed ID: 3842998
[No Abstract] [Full Text] [Related]
16. Deletion of 22q11 in two brothers with different phenotype.
Kasprzak L; Der Kaloustian VM; Elliott AM; Shevell M; Lejtenyi C; Eydoux P
Am J Med Genet; 1998 Jan; 75(3):288-91. PubMed ID: 9475599
[TBL] [Abstract][Full Text] [Related]
17. Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2).
Schuffenhauer S; Lichtner P; Peykar-Derakhshandeh P; Murken J; Haas OA; Back E; Wolff G; Zabel B; Barisic I; Rauch A; Borochowitz Z; Dallapiccola B; Ross M; Meitinger T
Eur J Hum Genet; 1998; 6(3):213-25. PubMed ID: 9781025
[TBL] [Abstract][Full Text] [Related]
18. Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p.
Lichtner P; AttiƩ-Bitach T; Schuffenhauer S; Henwood J; Bouvagnet P; Scambler PJ; Meitinger T; Vekemans M
J Mol Med (Berl); 2002 Jul; 80(7):431-42. PubMed ID: 12110949
[TBL] [Abstract][Full Text] [Related]
19. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH
Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
[TBL] [Abstract][Full Text] [Related]
20. The 22q11.2 deletion syndrome.
Emanuel BS; McDonald-McGinn D; Saitta SC; Zackai EH
Adv Pediatr; 2001; 48():39-73. PubMed ID: 11480765
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]