194 related articles for article (PubMed ID: 20727599)
21. Constitutional partial 1q trisomy mosaicism and Wilms tumor.
Mark HF; Wyandt H; Pan A; Milunsky JM
Cancer Genet Cytogenet; 2005 Oct; 162(2):166-71. PubMed ID: 16213366
[TBL] [Abstract][Full Text] [Related]
22. Phenotypic spectrum of interstitial 7p duplication in mosaic and non-mosaic forms.
Cox H; Stewart H; Hall L; Donnai D
Am J Med Genet; 2002 May; 109(4):306-10. PubMed ID: 11992485
[TBL] [Abstract][Full Text] [Related]
23. Cryptic mosaicism for monosomy 20 identified in renal tract cells.
Stefanou EG; Crocker M; Boon A; Stewart H
Clin Genet; 2006 Sep; 70(3):228-32. PubMed ID: 16922725
[TBL] [Abstract][Full Text] [Related]
24. Trisomy 14 mosaicism: a case report and review of the literature.
Lynch MF; Fernandes CJ; Shaffer LG; Potocki L
J Perinatol; 2004 Feb; 24(2):121-3. PubMed ID: 14762456
[TBL] [Abstract][Full Text] [Related]
25. Mosaic Trisomy 14 in a Newborn with Multiple Malformations: When Chromosomal Microarray is a Clue to Diagnosis.
Eventov-Friedman S; Frumkin A; Bar-Oz B; Raas-Rothschild A
Isr Med Assoc J; 2015 Jul; 17(7):459-60. PubMed ID: 26357728
[No Abstract] [Full Text] [Related]
26. Trisomy 14 mosaicism in a liveborn male: clinical report and review of the literature.
Kaplan LC; Wayne A; Crowell S; Latt SA
Am J Med Genet; 1986 Apr; 23(4):925-30. PubMed ID: 3515939
[TBL] [Abstract][Full Text] [Related]
27. Dental management of a child with trisomy 9 mosaicism: a case report.
Moskovitz M; Brener D; Annick RR
Pediatr Dent; 2006; 28(3):265-8. PubMed ID: 16805360
[TBL] [Abstract][Full Text] [Related]
28. Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.
Milunsky JM; Wyandt HE; Huang XL; Kang XZ; Elias ER; Milunsky A
Am J Med Genet; 1996 Jan; 61(3):269-73. PubMed ID: 8741873
[TBL] [Abstract][Full Text] [Related]
29. [Partial trisomy 12 and 8 with mosaicism, associated with translocation t(8;12) (p21;q13)].
Savary JB; Cousin J; Laï JL; Deminatti M
Ann Genet; 1977 Jun; 20(2):122-7. PubMed ID: 302686
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. A case of mosaic trisomy 14 due to an isochromosome, i(14q).
Ozawa N; Xu ZD; Soh K; Takabayashi T; Sato S; Yajima A; Suzuki M; Ikeuchi T; Tonomura A
Jinrui Idengaku Zasshi; 1984 Mar; 29(1):69-76. PubMed ID: 6748330
[No Abstract] [Full Text] [Related]
32. [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].
Turleau C; Rethoré MO; Junien C; Lejeune J; de Grouchy J
Ann Genet; 1979; 22(3):178-81. PubMed ID: 316677
[TBL] [Abstract][Full Text] [Related]
33. First report of mosaic trisomy 12 in a liveborn individual.
Patil SR; Bosch EP; Hanson JW
Am J Med Genet; 1983 Mar; 14(3):453-60. PubMed ID: 6859097
[TBL] [Abstract][Full Text] [Related]
34. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY
Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
[TBL] [Abstract][Full Text] [Related]
35. Delineation of a clinical syndrome caused by mosaic trisomy 15.
Bühler EM; Bienz G; Straumann E; Bösch N
Am J Med Genet; 1996 Mar; 62(2):109-12. PubMed ID: 8882390
[TBL] [Abstract][Full Text] [Related]
36. Trisomy 9 mosaicism syndrome. A case report and review of the literature.
Tarani L; Colloridi F; Raguso G; Rizzuti A; Bruni L; Tozzi MC; Palermo D; Panero A; Vignetti P
Ann Genet; 1994; 37(1):14-20. PubMed ID: 8010707
[TBL] [Abstract][Full Text] [Related]
37. New case of non-mosaic tetrasomy 9p in a severely polymalformed newborn girl.
de Azevedo Moreira LM; Freitas LM; Gusmão FA; Riegel M
Birth Defects Res A Clin Mol Teratol; 2003 Dec; 67(12):985-8. PubMed ID: 14745919
[TBL] [Abstract][Full Text] [Related]
38. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
Kulharya AS; Lovell CM; Flannery DB
Am J Med Genet; 2002 Dec; 113(4):367-70. PubMed ID: 12457409
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Proximal trisomy of 1q mosaicism in a girl with hypertrophic cardiomyopathy associated with Wolff-Parkinson-White syndrome and multiple congenital anomalies.
Hirshfeld AB; Thompson WR; Patel A; Boone LB; Murphy AM
Am J Med Genet; 2001 May; 100(4):264-8. PubMed ID: 11343316
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
