110 related articles for article (PubMed ID: 9541109)
21. Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
Knoll JH; Asamoah A; Pletcher BA; Wagstaff J
Am J Med Genet; 1995 Jan; 55(2):221-4. PubMed ID: 7717422
[TBL] [Abstract][Full Text] [Related]
22. Dental anomalies in Axenfeld-Rieger syndrome.
O'Dwyer EM; Jones DC
Int J Paediatr Dent; 2005 Nov; 15(6):459-63. PubMed ID: 16238657
[TBL] [Abstract][Full Text] [Related]
23. Clinical presentation of a variant of Axenfeld-Rieger syndrome associated with subtelomeric 6p deletion.
Martinez-Glez V; Lorda-Sanchez I; Ramirez JM; Ruiz-Barnes P; Rodriguez de Alba M; Diego-Alvarez D; Ramos C; Searby CC; Nishimura DY; Ayuso C
Eur J Med Genet; 2007; 50(2):120-7. PubMed ID: 17157569
[TBL] [Abstract][Full Text] [Related]
24. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
Gibson LH; McGrath J; Yang-Feng TL
Am J Med Genet; 1997 Feb; 68(4):417-20. PubMed ID: 9021014
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Evidence that Rieger syndrome maps to 4q25 or 4q27.
Vaux C; Sheffield L; Keith CG; Voullaire L
J Med Genet; 1992 Apr; 29(4):256-8. PubMed ID: 1583647
[TBL] [Abstract][Full Text] [Related]
27. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
Jin Y; Jin C; Wennerberg J; Mertens F; Höglund M
Cancer Res; 1998 Dec; 58(24):5859-65. PubMed ID: 9865746
[TBL] [Abstract][Full Text] [Related]
28. Characterization of a de novo balanced translocation t(9;18)(p23;q12.2) in a patient with oculoauriculovertebral spectrum.
Rooryck C; VuPhi Y; Souakri N; Burgelin I; Saura R; Lacombe D; Arveiler B; Taine L
Eur J Med Genet; 2010; 53(2):104-7. PubMed ID: 20132917
[TBL] [Abstract][Full Text] [Related]
29. Karyotyping human chromosomes by combinatorial multi-fluor FISH.
Speicher MR; Gwyn Ballard S; Ward DC
Nat Genet; 1996 Apr; 12(4):368-75. PubMed ID: 8630489
[TBL] [Abstract][Full Text] [Related]
30. Rieger syndrome and interstitial 4q26 deletion.
Fryns JP; Van Den Berghe H
Genet Couns; 1992; 3(3):153-4. PubMed ID: 1388934
[No Abstract] [Full Text] [Related]
31. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P
Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603
[TBL] [Abstract][Full Text] [Related]
32. Subchromosomal band interval mapping and ordering of DNA markers in the region 3q26.3-q27 involved in the dup(3q) syndrome.
Rizzu P; Baldini A
Genomics; 1994 Dec; 24(3):580-2. PubMed ID: 7713511
[TBL] [Abstract][Full Text] [Related]
33. Different manifestation of Rieger syndrome in monozygotic twins.
Geyer O; Loewenstein A; Garty BZ; Lazar M
J Pediatr Ophthalmol Strabismus; 1994; 31(1):57-8. PubMed ID: 8195966
[No Abstract] [Full Text] [Related]
34. Familial complex chromosome rearrangement ascertained by in situ hybridisation.
Fuster C; Miguez L; Miró R; Rigola MA; Perez A; Egozcue J
J Med Genet; 1997 Feb; 34(2):164-6. PubMed ID: 9039997
[TBL] [Abstract][Full Text] [Related]
35. Cytogenetic findings indicate heterogeneity in patients with blepharophimosis, epicanthus inversus, and developmental delay.
Warburg M; Bugge M; Brøndum-Nielsen K
J Med Genet; 1995 Jan; 32(1):19-24. PubMed ID: 7897621
[TBL] [Abstract][Full Text] [Related]
36. Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization.
Sawyer JR; Swanson CM; Wheeler G; Cunniff C
Am J Med Genet; 1995 Mar; 56(2):203-9. PubMed ID: 7625446
[TBL] [Abstract][Full Text] [Related]
37. Cytogenetic characterization of cat eye syndrome marker chromosome.
Wenger SL; Surti U; Nwokoro NA; Steele MW
Ann Genet; 1994; 37(1):33-6. PubMed ID: 8010712
[TBL] [Abstract][Full Text] [Related]
38. Establishment of an R-banded rabbit karyotype nomenclature by FISH localization of 23 chromosome-specific genes on both G- and R-banded chromosomes.
Hayes H; Rogel-Gaillard C; Zijlstra C; De Haan NA; Urien C; Bourgeaux N; Bertaud M; Bosma AA
Cytogenet Genome Res; 2002; 98(2-3):199-205. PubMed ID: 12698004
[TBL] [Abstract][Full Text] [Related]
39. Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization analyses.
Sáez B; Martín-Subero JI; Largo C; Martín MC; Odero MD; Prosper F; Siebert R; Calasanz MJ; Cigudosa JC
Cancer Genet Cytogenet; 2006 Sep; 169(2):143-9. PubMed ID: 16938572
[TBL] [Abstract][Full Text] [Related]
40. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]