179 related articles for article (PubMed ID: 22537675)
21. A new association of congenital hydrocephalus, albinism, megalocornea, and retinal coloboma in a syndromic child: a clinical and genetic study.
Dubé P; Der Kaloustian VM ; Demczuk S; Saabti H; Koenekoop RK
Ophthalmic Genet; 2000 Dec; 21(4):211-6. PubMed ID: 11135491
[TBL] [Abstract][Full Text] [Related]
22. Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23-pter.
Gruchy N; Jacquemont ML; Lyonnet S; Labrune P; El Kamel I; Siffroi JP; Portnoï MF
Am J Med Genet A; 2007 Oct; 143A(20):2417-22. PubMed ID: 17853488
[TBL] [Abstract][Full Text] [Related]
23. Translocation/duplication of 9p onto a duplicated 4q.
Rivera H; Figuera LE; Vasquez AI
Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
[TBL] [Abstract][Full Text] [Related]
24. [Trisomy 9p. Report of two new cases].
San Román Muñoz M; Herranz Fernández JL; Tejerina Puente A; Arteaga Manjón-Cabeza R; López Grondona F
An Pediatr (Barc); 2004 Oct; 61(4):336-9. PubMed ID: 15456590
[TBL] [Abstract][Full Text] [Related]
25. Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGH.
Utine EG; Alanay Y; Aktas D; Alikasifoglu M; Boduroglu K; Vermeesch J; Tuncbilek E; Fryns JP
Eur J Med Genet; 2008; 51(4):343-50. PubMed ID: 18440888
[TBL] [Abstract][Full Text] [Related]
26. An additional case of 9p syndrome.
Latos-Bielenska A; Krawczynski M; Ignys I; Wolnik-Brzozowska D
Acta Anthropogenet; 1983; 7(4):391-5. PubMed ID: 6680318
[TBL] [Abstract][Full Text] [Related]
27. Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23.
Kawara H; Yamamoto T; Harada N; Yoshiura K; Niikawa N; Nishimura A; Mizuguchi T; Matsumoto N
Am J Med Genet A; 2006 Feb; 140(4):373-7. PubMed ID: 16419130
[TBL] [Abstract][Full Text] [Related]
28. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
Repetto GM; Wagstaff J; Korf BR; Knoll JH
Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094
[TBL] [Abstract][Full Text] [Related]
29. "Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.
Zollino M; Wright TJ; Di Stefano C; Tosolini A; Battaglia A; Altherr MR; Neri G
Am J Med Genet; 1999 Feb; 82(5):371-5. PubMed ID: 10069706
[TBL] [Abstract][Full Text] [Related]
30. [A case of 9p-syndrome identified chromosome 20 on chromosome 9p by M-FISH].
Koseki N; Obara Y; Ookawa A; Katsumi M; Funato T; Kaku M
Rinsho Byori; 2001 Oct; 49(10):1045-8. PubMed ID: 11769470
[TBL] [Abstract][Full Text] [Related]
31. Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation.
Tayel SM; Kurczynski TW; Casperson S; McCorquodale MM
Am J Med Genet; 1988 Dec; 31(4):853-61. PubMed ID: 3239578
[TBL] [Abstract][Full Text] [Related]
32. 20-Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: narrowing of the 9p duplication critical region to 6 Mb.
Bonaglia MC; Giorda R; Carrozzo R; Roncoroni ME; Grasso R; Borgatti R; Zuffardi O
Am J Med Genet; 2002 Oct; 112(2):154-9. PubMed ID: 12244548
[TBL] [Abstract][Full Text] [Related]
33. Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature.
Ballarati L; Cereda A; Caselli R; Selicorni A; Recalcati MP; Maitz S; Finelli P; Larizza L; Giardino D
Eur J Med Genet; 2011; 54(1):55-9. PubMed ID: 20969981
[TBL] [Abstract][Full Text] [Related]
34. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
35. De novo inverted duplication 9p21pter involving telomeric repeated sequences.
Sanlaville D; Baumann C; Lapierre JM; Romana S; Collot N; Cacheux V; Turleau C; Tachdjian G
Am J Med Genet; 1999 Mar; 83(2):125-31. PubMed ID: 10190483
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Phenotype-genotype correlation of a patient with a "balanced" translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion.
Papadopoulou E; Sismani C; Christodoulou C; Ioannides M; Kalmanti M; Patsalis P
Am J Med Genet A; 2010 Jun; 152A(6):1515-22. PubMed ID: 20503328
[TBL] [Abstract][Full Text] [Related]
38. Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.
Di Giacomo MC; Cesarano C; Bukvic N; Manisali E; Guanti G; Susca F
Prenat Diagn; 2004 Aug; 24(8):619-22. PubMed ID: 15305349
[TBL] [Abstract][Full Text] [Related]
39. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
[TBL] [Abstract][Full Text] [Related]
40. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
Murru D; Boccone L; Ristaldi MS; Nucaro AL
Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
