570 related articles for article (PubMed ID: 16683276)
1. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
Prontera P; Buldrini B; Aiello V; Gruppioni R; Bonfatti A; Venti G; Ferlini A; Sensi A; Calzolari E; Donti E
Prenat Diagn; 2006 Jun; 26(6):571-6. PubMed ID: 16683276
[TBL] [Abstract][Full Text] [Related]
2. Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
Chen CP; Huang HK; Su YN; Chern SR; Su JW; Lee CC; Town DD; Chen WL; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2012 Mar; 51(1):77-82. PubMed ID: 22482973
[TBL] [Abstract][Full Text] [Related]
3. A familial reciprocal translocation t(1;15) in three generations identified in a regular trisomy 21 patient.
García-Delgado C; Bahena-Martínez E; Aparicio-Onofre A; Guevara-Yañez R; Cervantes-Peredo A; Azotla-Vilchis OC; Estrada-Mena J; Luna-Angulo A; Villa-Morales J; Moran-Barroso VF
Genet Couns; 2010; 21(3):299-306. PubMed ID: 20964121
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of trisomy 3 mosaicism.
Zaslav AL; Pierno G; Davis J; Fougner A; Jacob J; Kazi R; Blumenthal D; Sturim S; Shaham M; Fox J
Prenat Diagn; 2004 Sep; 24(9):693-6. PubMed ID: 15386452
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
Santolaya-Forgas J; De Leon J; Powell WC; Tonk V
Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
[TBL] [Abstract][Full Text] [Related]
7. The clinical application of interphase FISH in prenatal diagnosis.
Pergament E; Chen PX; Thangavelu M; Fiddler M
Prenat Diagn; 2000 Mar; 20(3):215-20. PubMed ID: 10719324
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
Senger G; Chudoba I; Friedrich U; Tommerup N; Claussen U; Brøndum-Nielsen K
Prenat Diagn; 1997 Apr; 17(4):369-74. PubMed ID: 9160390
[TBL] [Abstract][Full Text] [Related]
9. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.
Chen CP; Chern SR; Chen YN; Wu PS; Yang CW; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2015 Aug; 54(4):426-31. PubMed ID: 26384064
[TBL] [Abstract][Full Text] [Related]
10. A family with segregation of an unbalanced translocation (7;13) (q36;q32) in three patients with severe mental retardation, microcephaly and dysmorphic features, detected by subtelomere FISH: genetic counselling and prenatal diagnosis.
Nucaro A; Crisponi G; Minafra L; Rossino R; Cianchetti C
Genet Couns; 2008; 19(1):37-42. PubMed ID: 18564499
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
12. [Marker chromosomes as a product of familial translocation (11;22) identified with molecular cytogenetic methods].
Stankiewicz P; Korniszewski L; Bocian E; Stańczak H
Pediatr Pol; 1996 Mar; 71(3):241-5. PubMed ID: 8966096
[TBL] [Abstract][Full Text] [Related]
13. [Trisomy of the distal 15q region due to familial balanced translocation t(15;16)(q24;p13) and unusual mosaicism in the mother of the proband].
Nazarenko SA; Nazarenko LP; Baranova VA
Tsitol Genet; 1987; 21(6):434-7. PubMed ID: 3445362
[TBL] [Abstract][Full Text] [Related]
14. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
[TBL] [Abstract][Full Text] [Related]
15. Structural chromosomal mosaicism and prenatal diagnosis.
Pipiras E; Dupont C; Chantot-Bastaraud S; Siffroi JP; Bucourt M; Batallan A; Largillière C; Uzan M; Wolf JP; Benzacken B
Prenat Diagn; 2004 Feb; 24(2):101-3. PubMed ID: 14974115
[TBL] [Abstract][Full Text] [Related]
16. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
Bacino CA; Kashork CD; Davino NA; Shaffer LG
Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
[TBL] [Abstract][Full Text] [Related]
17. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
Donaghue C; Mann K; Docherty Z; Ogilvie CM
Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.
Chen CP; Chen M; Pan YJ; Su YN; Chern SR; Tsai FJ; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2011 Sep; 50(3):331-8. PubMed ID: 22030049
[TBL] [Abstract][Full Text] [Related]
19. Prenatally diagnosed trisomy 6 mosaicism.
Gupta N; Pradhan M; Manisha ; Singh R; Phadke SR
Prenat Diagn; 2004 Oct; 24(10):841-4. PubMed ID: 15503282
[No Abstract] [Full Text] [Related]
20. A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome.
Roberts E; Dunlop J; Davis GS; Churchill D; Davison EV
Prenat Diagn; 2003 Jul; 23(7):564-5. PubMed ID: 12868084
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
