336 related articles for article (PubMed ID: 10820405)
1. 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]
2. 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]
3. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
4. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
[TBL] [Abstract][Full Text] [Related]
5. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
[TBL] [Abstract][Full Text] [Related]
6. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
Vorsanova SG; Yurov YB; Brusquant D; Carles E; Roizes G
Tsitol Genet; 2002; 36(1):46-9. PubMed ID: 12012596
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.
Faivre L; Morichon-Delvallez N; Viot G; Larget-Piet A; Narcy F; Turleau C; Pinson MP; Dumez Y; Munnich A; Vekemans M
Prenat Diagn; 1999 Mar; 19(3):282-6. PubMed ID: 10210132
[TBL] [Abstract][Full Text] [Related]
9. Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.
Pettenati MJ; Jackle B; Bobby P; Stewart W; Von Kap-Herr C; Mowrey P; Rao PN; May KM
Am J Med Genet; 2002 Jul; 111(1):48-53. PubMed ID: 12124733
[TBL] [Abstract][Full Text] [Related]
10. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
Qumsiyeh MB; Stevens CA
Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
[TBL] [Abstract][Full Text] [Related]
11. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
12. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation.
Migliori MV; Pettinari A; Ciaschini AM; Piermattei P; Pigliapoco F; Discepoli G
Prenat Diagn; 2004 Apr; 24(4):290-2. PubMed ID: 15065104
[TBL] [Abstract][Full Text] [Related]
14. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
Velissariou V; Sismani C; Christopoulou S; Kaminopetros P; Hatzaki A; Evangelidou P; Koumbaris G; Bartsocas CS; Stylianidou G; Skordis N; Diakoumakos A; Patsalis PC
Eur J Med Genet; 2007; 50(4):291-300. PubMed ID: 17584536
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
Prontera P; Aiello V; Toschi M; Turci A; Gruppioni R; Buldrini B; Zago S; Bonfatti A; Donti E; Calzolari E; Sensi A
Genet Couns; 2007; 18(3):309-15. PubMed ID: 18019372
[TBL] [Abstract][Full Text] [Related]
16. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
Zhao L; Li H; Xue YQ; Pan JL; Wu YF; Lu M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):611-4. PubMed ID: 15583994
[TBL] [Abstract][Full Text] [Related]
17. Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.
Popp S; Schulze B; Granzow M; Keller M; Holtgreve-Grez H; Schoell B; Brough M; Hager HD; Tariverdian G; Brown J; Kearney L; Jauch A
Hum Genet; 2002 Jul; 111(1):31-9. PubMed ID: 12136233
[TBL] [Abstract][Full Text] [Related]
18. Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosis.
Mohandas T; Canning N; Chu W; Passage MB; Anderson CE; Kaback MM
Am J Med Genet; 1985 Feb; 20(2):361-8. PubMed ID: 2579555
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]