140 related articles for article (PubMed ID: 19664845)
1. Partial mosaic trisomy 5: a new case report with ocular involvement.
Schlegel Z; Valent A; Hirsch A
J Fr Ophtalmol; 2009 Oct; 32(8):533-9. PubMed ID: 19664845
[TBL] [Abstract][Full Text] [Related]
2. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
3. Duplication of 5q15-q23.2: case report and literature review.
Douyard J; Hawley P; Shaham M; Kimonis V
Birth Defects Res A Clin Mol Teratol; 2006 Apr; 76(4):272-6. PubMed ID: 16602097
[TBL] [Abstract][Full Text] [Related]
4. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Melo JB; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch JR; Kosyakova N; Ewers E; Liehr T; Carreira IM
Cytogenet Genome Res; 2009; 125(2):109-14. PubMed ID: 19729913
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Trisomy 9 syndrome: report of a case with Crohn disease and review of the literature.
Wooldridge J; Zunich J
Am J Med Genet; 1995 Apr; 56(3):258-64. PubMed ID: 7778585
[TBL] [Abstract][Full Text] [Related]
7. A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.
Karaoguz MY; Biri A; Pala E; Kan D; Poyraz A; Kurdoglu M; Percin EF
Genet Couns; 2006; 17(2):197-204. PubMed ID: 16970038
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Ocular defects associated with a duplication of the distal part of the long arm of chromosome 1: a case report].
Le Goff L; Hadjadj E; Denis D
J Fr Ophtalmol; 2002 Apr; 25(4):388-92. PubMed ID: 12011743
[TBL] [Abstract][Full Text] [Related]
10. Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicism.
Spinner NB; Grace KR; Owens NL; Sovinsky L; Pellegrino JE; McDonald-McGinn D; Zackai E
Am J Med Genet; 1995 Mar; 56(1):22-4. PubMed ID: 7747780
[TBL] [Abstract][Full Text] [Related]
11. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
[TBL] [Abstract][Full Text] [Related]
12. Distal partial trisomy 1q: report of two cases and a review of the literature.
Utine GE; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
[TBL] [Abstract][Full Text] [Related]
13. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
Kosaki R; Hanai S; Kakishima H; Okada MA; Hayashi S; Ito Y; Takahashi T; Kosaki K; Okuyama T
Congenit Anom (Kyoto); 2006 Jun; 46(2):115-7. PubMed ID: 16732770
[TBL] [Abstract][Full Text] [Related]
14. PARTIAL TRISOMY 5p12-q 11.2 RESULTING FROM A MARKER CHROMOSOME: A NEW CASE REPORT WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER.
Erdem HB; Sahin I; Tasdemir S; Tatar A
Genet Couns; 2016; 27(3):295-303. PubMed ID: 30204959
[TBL] [Abstract][Full Text] [Related]
15. Maternal uniparental isodisomy 10 and mosaicism for an additional marker chromosome derived from the paternal chromosome 10 in a fetus.
Schlegel M; Baumer A; Riegel M; Wiedemann U; Schinzel A
Prenat Diagn; 2002 May; 22(5):418-21. PubMed ID: 12001199
[TBL] [Abstract][Full Text] [Related]
16. Trisomy 6q syndrome: a case with a << de novo >> 6q23 tandem duplication.
Causio F; Fischetto R; Carnevale F; Pansini A; Rocchi M
Genet Couns; 2001; 12(2):145-50. PubMed ID: 11491309
[TBL] [Abstract][Full Text] [Related]
17. Histopathology and molecular cytogenetics of a corneal opacity associated with the trisomy 8 mosaic syndrome (46,XY/47,XY, +8).
Scott JA; Howard PJ; Smith PA; Fryer A; Easty DL; Patterson A; Kaye SB
Cornea; 1997 Jan; 16(1):35-41. PubMed ID: 8985632
[TBL] [Abstract][Full Text] [Related]
18. Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?
Reish O; Wolach B; Amiel A; Kedar I; Dolfin T; Fejgin M
Am J Med Genet; 1998 Apr; 77(1):72-5. PubMed ID: 9557898
[TBL] [Abstract][Full Text] [Related]
19. M-FISH applications in clinical genetics.
Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
[TBL] [Abstract][Full Text] [Related]
20. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
Crowe CA; Schwartz S; Black CJ; Jaswaney V
Am J Med Genet; 1997 Sep; 71(4):406-13. PubMed ID: 9286446
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]