254 related articles for article (PubMed ID: 1296516)
1. Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patients.
Obregon MG; Mingarelli R; Digilio MC; Zelante L; Giannotti A; Sabatino G; Dallapiccola B
Ann Genet; 1992; 35(4):208-12. PubMed ID: 1296516
[TBL] [Abstract][Full Text] [Related]
2. 11q- syndrome: three cases and a review of the literature.
Leegte B; Kerstjens-Frederikse WS; Deelstra K; Begeer JH; van Essen AJ
Genet Couns; 1999; 10(3):305-13. PubMed ID: 10546104
[TBL] [Abstract][Full Text] [Related]
3. [Clinical picture of partial monosomy of chromosome 11 q].
Dörr U
Monatsschr Kinderheilkd; 1986 Nov; 134(11):808-11. PubMed ID: 3807920
[TBL] [Abstract][Full Text] [Related]
4. Interstitial deletion 11q. Case report and review of the literature.
De Pater JM; Ippel PF; Bijlsma JB; Van Nieuwenhuizen O
Genet Couns; 1997; 8(4):335-9. PubMed ID: 9457504
[TBL] [Abstract][Full Text] [Related]
5. Distal 11q deletion: a specific clinical entity.
Fryns JP; Kleczkowska A; Smeets E; Van den Berghe H
Helv Paediatr Acta; 1987 Oct; 42(2-3):191-4. PubMed ID: 3692885
[TBL] [Abstract][Full Text] [Related]
6. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
[TBL] [Abstract][Full Text] [Related]
7. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33).
Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N
Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of deletion 11q23-->qter. Report of two unrelated cases.
Caiola A; Altissimi D; Brinchi V; Maggi E; Mingarelli R
Ann Genet; 1993; 36(4):228-30. PubMed ID: 8166431
[TBL] [Abstract][Full Text] [Related]
9. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
[TBL] [Abstract][Full Text] [Related]
10. Jacobsen syndrome: chromosome deletion at 11q23.
Clang DR; LaBaere RJ
J Am Osteopath Assoc; 1998 Oct; 98(10):551-4. PubMed ID: 9821738
[TBL] [Abstract][Full Text] [Related]
11. [Deletion 11q23 --> qter (Jacobsen Syndrome) associated with duodenal atresia and annular pancreas].
Fernández González N; Prieto Espuñes S; Ibáñez Fernández A; Fernández Colomer B; López Sastre J; Fernández Toral J
An Esp Pediatr; 2002 Sep; 57(3):249-52. PubMed ID: 12199949
[TBL] [Abstract][Full Text] [Related]
12. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
13. The 18p- syndrome. Report of five cases.
Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
[TBL] [Abstract][Full Text] [Related]
14. [The (18)(q 22----qter) deletion in patients with complete clinical features of the De Grouchy syndrome].
Vranjesević D; Dukić S; Jović N; Branković S; Kosanović M
Neurol Croat; 1991; 40(1):39-47. PubMed ID: 2070033
[TBL] [Abstract][Full Text] [Related]
15. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
Wieczorek D; Krause M; Majewski F; Albrecht B; Horn D; Riess O; Gillessen-Kaesbach G
Eur J Hum Genet; 2000 Jul; 8(7):519-26. PubMed ID: 10909852
[TBL] [Abstract][Full Text] [Related]
16. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
[TBL] [Abstract][Full Text] [Related]
17. Deletion of the distal long arm of chromosome 1: a definable syndrome.
Johnson VP; Heck LJ; Carter GA; Flom JO
Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
[TBL] [Abstract][Full Text] [Related]
18. Del(4)(pter-->q33:) case report and review of the literature.
Grammatico P; Spaccini L; Di Rosa C; Cupilari F; Del Porto G
Genet Couns; 1997; 8(1):39-42. PubMed ID: 9101277
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletion of (17)(p11.2). A microdeletion syndrome. Another example.
de Almeida JC; Reis DF; Martins RR
Ann Genet; 1989; 32(3):184-6. PubMed ID: 2817780
[TBL] [Abstract][Full Text] [Related]
20. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
Dobyns WB; Dewald GW; Carlson RO; Mair DD; Michels VV
Am J Med Genet; 1985 Sep; 22(1):125-34. PubMed ID: 3901750
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
