110 related articles for article (PubMed ID: 9541109)
1. A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome.
Ogilvie CM; Raymond FL; Harrison RH; Scriven PN; Docherty Z
J Med Genet; 1998 Mar; 35(3):234-7. PubMed ID: 9541109
[TBL] [Abstract][Full Text] [Related]
2. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
Spikes AS; Hegmann K; Smith JL; Shaffer LG
Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
[TBL] [Abstract][Full Text] [Related]
3. De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies.
Wakita Y; Narahara K; Tsuji K; Yokoyama Y; Ninomiya S; Murakami R; Kikkawa K; Seino Y
Hum Genet; 1992 Mar; 88(5):596-8. PubMed ID: 1551663
[TBL] [Abstract][Full Text] [Related]
4. A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature.
Becker SA; Popp S; Rager K; Jauch A
Eur J Pediatr; 2003 Apr; 162(4):267-70. PubMed ID: 12647202
[TBL] [Abstract][Full Text] [Related]
5. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
Peschka B; Leygraaf J; Hansmann D; Hansmann M; Schröck E; Ried T; Engels H; Schwanitz G; Schubert R
Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433
[TBL] [Abstract][Full Text] [Related]
6. Multipaint FISH: a rapid and reliable way to define cryptic and complex abnormalities.
Joyce CA; Ross FM; Dennis NR; Wyre ND; Barber JC
Clin Genet; 1999 Sep; 56(3):192-9. PubMed ID: 10563478
[TBL] [Abstract][Full Text] [Related]
7. Delineation of complex chromosomal rearrangements: evidence for increased complexity.
Astbury C; Christ LA; Aughton DJ; Cassidy SB; Fujimoto A; Pletcher BA; Schafer IA; Schwartz S
Hum Genet; 2004 Apr; 114(5):448-57. PubMed ID: 14767757
[TBL] [Abstract][Full Text] [Related]
8. Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).
Makita Y; Masuno M; Imaizumi K; Yamashita S; Ohba S; Ito D; Kuroki Y
Am J Med Genet; 1995 May; 57(1):19-21. PubMed ID: 7645592
[TBL] [Abstract][Full Text] [Related]
9. Rieger syndrome: a case report.
Dimitrakopoulos J; Voyatzis N; Katopodi T
J Oral Maxillofac Surg; 1997 May; 55(5):517-21. PubMed ID: 9146524
[No Abstract] [Full Text] [Related]
10. Disclosure of five breakpoints in a complex chromosome rearrangement by microdissection and FISH.
Engelen JJ; Loots WJ; Albrechts JC; Motoh PC; Fryns JP; Hamers AJ; Geraedts JP
J Med Genet; 1996 Jul; 33(7):562-6. PubMed ID: 8818941
[TBL] [Abstract][Full Text] [Related]
11. Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies.
Thienpont B; Gewillig M; Fryns JP; Devriendt K; Vermeesch J
Cytogenet Genome Res; 2006; 114(3-4):338-41. PubMed ID: 16954676
[TBL] [Abstract][Full Text] [Related]
12. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
Wang H; McLaughlin M; Thompson C; Hunter AG
Am J Med Genet; 1993 Jun; 46(5):559-62. PubMed ID: 8322821
[TBL] [Abstract][Full Text] [Related]
13. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
14. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
15. A second locus for Rieger syndrome maps to chromosome 13q14.
Phillips JC; del Bono EA; Haines JL; Pralea AM; Cohen JS; Greff LJ; Wiggs JL
Am J Hum Genet; 1996 Sep; 59(3):613-9. PubMed ID: 8751862
[TBL] [Abstract][Full Text] [Related]
16. FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.
Phelan MC; Blackburn W; Rogers RC; Crawford EC; Cooley NR; Schrock E; Ning Y; Ried T
Prenat Diagn; 1998 Nov; 18(11):1174-80. PubMed ID: 9854728
[TBL] [Abstract][Full Text] [Related]
17. Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints.
McTaggart KE; Budarf ML; Driscoll DA; Emanuel BS; Ferreira P; McDermid HE
Cytogenet Cell Genet; 1998; 81(3-4):222-8. PubMed ID: 9730608
[TBL] [Abstract][Full Text] [Related]
18. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping.
Veldman T; Vignon C; Schröck E; Rowley JD; Ried T
Nat Genet; 1997 Apr; 15(4):406-10. PubMed ID: 9090389
[TBL] [Abstract][Full Text] [Related]
19. A de novo Pericentric Inversion in Chromosome 4 Associated with Disruption of PITX2 and a Microdeletion in 4p15.2 in a Patient with Axenfeld-Rieger Syndrome and Developmental Delay.
Maldžienė Ž; Preikšaitienė E; Ignotienė S; Kapitanova N; Utkus A; Kučinskas V
Cytogenet Genome Res; 2017; 151(1):5-9. PubMed ID: 28226328
[TBL] [Abstract][Full Text] [Related]
20. [The Rieger syndrome. A clinical study. A study of 4 generations in one family with the Rieger syndrome].
Rusu V
Oftalmologia; 1997; 41(3):234-7. PubMed ID: 9409970
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
