191 related articles for article (PubMed ID: 16683274)
1. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
Mercier S; Fellmann F; Cattin J; Bresson JL
Prenat Diagn; 1996 Nov; 16(11):1046-50. PubMed ID: 8953640
[TBL] [Abstract][Full Text] [Related]
3. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
Ruiz C; Grubs RE; Jewett T; Cox-Jones K; Abruzzese E; Pettenati MJ; Rao PN
Am J Med Genet; 1996 Aug; 64(3):478-84. PubMed ID: 8862625
[TBL] [Abstract][Full Text] [Related]
4. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangements.
Cotter PD; Caggana M; Willner JP; Babu A; Desnick RJ
Am J Med Genet; 1996 Dec; 66(2):197-9. PubMed ID: 8958330
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 10p duplication characterized by fluorescence in situ hybridization.
Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
[TBL] [Abstract][Full Text] [Related]
8. Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.
Michalski K; Rauer M; Williamson N; Perszyk A; Hoo JJ
Am J Med Genet; 1993 Apr; 46(1):88-94. PubMed ID: 8494036
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Combined use of cytogenetic analysis and FISH for the identification of two antenatal de novo markers as Robertsonian translocations involving the p arms.
Pierluigi M; Battaglia P; Perfumo C; Baroncini A; Bricarelli FD
Ann Genet; 1997; 40(2):99-103. PubMed ID: 9259956
[TBL] [Abstract][Full Text] [Related]
11. [Cytogenic characterization of chromosome markers detected at amniocentesis: implications for karyotype-phenotype correlations].
Valerio D; Aiello R; Altieri V; Antonucci F
Minerva Ginecol; 1996 Sep; 48(9):365-9. PubMed ID: 8999384
[TBL] [Abstract][Full Text] [Related]
12. A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.
Gibson LH; McGrath J; Yang-Feng TL
Am J Med Genet; 1997 Feb; 68(4):417-20. PubMed ID: 9021014
[TBL] [Abstract][Full Text] [Related]
13. Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.
Darnaude MT; Diaz de Bustamante A; Cabello P; Vallcorba I
Ann Genet; 1996; 39(2):61-3. PubMed ID: 8766134
[TBL] [Abstract][Full Text] [Related]
14. Balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
Farrell SA; Summers AM; Gardner HA; Uchida IA
Am J Med Genet; 1994 Sep; 52(3):360-1. PubMed ID: 7810570
[No Abstract] [Full Text] [Related]
15. Complex familial rearrangement of chromosome 9p24.3 detected by FISH.
Repetto GM; Wagstaff J; Korf BR; Knoll JH
Am J Med Genet; 1998 Apr; 76(4):306-9. PubMed ID: 9545094
[TBL] [Abstract][Full Text] [Related]
16. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
Fryns JP; Kleczkowska A; Kenis H
Ann Genet; 1984; 27(1):62-4. PubMed ID: 6609678
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of minute 5p- deletion: a cytogenetic problem in detection.
Benn PA; Hsu LY; Verma RS; Alonso ML; Reich E; Wishnick M
Obstet Gynecol; 1987 Sep; 70(3 Pt 2):449-52. PubMed ID: 3627600
[TBL] [Abstract][Full Text] [Related]
18. Microdissection and DOP-PCR-based reverse chromosome painting as a fast and reliable strategy in the analysis of various structural chromosome abnormalities.
Müller-Navia J; Nebel A; Oehler D; Theile U; Zabel B; Schleiermacher E
Prenat Diagn; 1996 Oct; 16(10):915-22. PubMed ID: 8938060
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus.
Chen CP; Liu FF; Jan SW; Yang YC; Lan CC
Prenat Diagn; 1996 Dec; 16(12):1137-40. PubMed ID: 8994250
[TBL] [Abstract][Full Text] [Related]
20. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
