487 related articles for article (PubMed ID: 10191430)
1. 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]
2. 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]
3. 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]
4. The 22q11.2 deletion syndrome: more answers but more questions.
Fernhoff PM
J Pediatr; 2000 Aug; 137(2):145-7. PubMed ID: 10931401
[No 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. 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]
7. 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]
8. 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]
9. 22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes.
Vincent MC; Heitz F; Tricoire J; Bourrouillou G; Kuhlein E; Rolland M; Calvas P
Genet Couns; 1999; 10(1):43-9. PubMed ID: 10191428
[TBL] [Abstract][Full Text] [Related]
10. The deletions of 22q11--the Portuguese experience.
Gaspar IM; Lourenço MT; Reis MI; Soares MA; Nogueira G; Ferreira F; Feijóo MJ
Genet Couns; 1999; 10(1):51-7. PubMed ID: 10191429
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.
Lipson A; Fagan K; Colley A; Colley P; Sholler G; Issacs D; Oates RK
Am J Med Genet; 1996 Nov; 65(4):304-8. PubMed ID: 8923940
[TBL] [Abstract][Full Text] [Related]
13. Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
Vantrappen G; Devriendt K; Swillen A; Rommel N; Vogels A; Eyskens B; Gewillig M; Feenstra L; Fryns JP
Genet Couns; 1999; 10(1):3-9. PubMed ID: 10191424
[TBL] [Abstract][Full Text] [Related]
14. Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications.
Verri A; Maraschio P; Devriendt K; Uggetti C; Spadoni E; Haeusler E; Federico A
Ann Genet; 2004; 47(3):281-7. PubMed ID: 15337474
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Partial deletion 10p syndrome. Report of two patients.
Obregon MG; Mingarelli R; Giannotti A; di Comite A; Spedicato FS; Dallapiccola B
Ann Genet; 1992; 35(2):101-4. PubMed ID: 1524405
[TBL] [Abstract][Full Text] [Related]
18. [DiGeorge syndrome, a review of 52 patients].
Minier F; Carles D; Pelluard F; Alberti EM; Stern L; Saura R
Arch Pediatr; 2005 Mar; 12(3):254-7. PubMed ID: 15734119
[TBL] [Abstract][Full Text] [Related]
19. [Phenotypic variability: genetics and chance--deletion 22q11 and schizophrenia].
Breuning MH
Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2016-9. PubMed ID: 12428459
[TBL] [Abstract][Full Text] [Related]
20. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome].
Pânzaru M; Rusu C; Voloşciuc M; Braha E; Butnariu L; Ivanov I; Grămescu M; Popescu R; Caba L; Sireteanu A; Macovei M; Covic M; Gorduza EV
Rev Med Chir Soc Med Nat Iasi; 2011; 115(3):756-61. PubMed ID: 22046783
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
