490 related articles for article (PubMed ID: 12424755)
1. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
Kímya Y; Yakut T; Egelí U; Ozerkan K
Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
[TBL] [Abstract][Full Text] [Related]
2. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
[TBL] [Abstract][Full Text] [Related]
3. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J
Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
[TBL] [Abstract][Full Text] [Related]
4. Trisomy (1q)(q42----qter): confirmation of a syndrome.
Chia NL; Bousfield LR; Poon CC; Trudinger BJ
Clin Genet; 1988 Oct; 34(4):224-9. PubMed ID: 3233776
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
Duba HC; Erdel M; Löffler J; Bereuther L; Fischer H; Utermann B; Utermann G
J Med Genet; 1997 Apr; 34(4):309-13. PubMed ID: 9138155
[TBL] [Abstract][Full Text] [Related]
8. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome.
Peng HH; Wang TH; Hsueh DW; Chang SD; Soong YK
Prenat Diagn; 2005 Jun; 25(6):470-4. PubMed ID: 15966037
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of de novo trisomy 1(q21-qter)der(Y)t(Y;1) in a malformed live born.
Fernández-Novoa MC; Vargas MT; Granell MR; Carreto P
Prenat Diagn; 2004 Jun; 24(6):414-7. PubMed ID: 15229838
[TBL] [Abstract][Full Text] [Related]
12. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. High resolution replication banding combined with in situ hybridization for the delineation of a subtle chromosome rearrangement.
Qumsiyeh MB; Wilroy RS; Peeden JN; Tharapel AT
Am J Med Genet; 1991 Oct; 41(1):99-101. PubMed ID: 1719815
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
