315 related articles for article (PubMed ID: 10360520)
1. Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping.
Ning Y; Laundon CH; Schröck E; Buchanan P; Ried T
Prenat Diagn; 1999 May; 19(5):480-2. PubMed ID: 10360520
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Prenatal diagnosis of mosaic tetrasomy 5p.
Park JP; Barefoot KH; Ornvold K; Berg SZ; Dossu JR; Mohandas TK
Prenat Diagn; 2001 May; 21(5):351-3. PubMed ID: 11360274
[TBL] [Abstract][Full Text] [Related]
4. [Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells].
Marguerat P; Gaide AC; Thonney F; Schorderet D
Rev Med Suisse Romande; 2000 May; 120(5):401-7. PubMed ID: 10911743
[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. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
Hsieh LJ; Hsieh TC; Yeh GP; Lin MI; Chen M; Wang BB
Fetal Diagn Ther; 2004; 19(4):356-60. PubMed ID: 15192296
[TBL] [Abstract][Full Text] [Related]
7. A case of mosaic tetrasomy 12p (Pallister-Killian Syndrome) diagnosed prenatally: comparison of chromosome analyses of various cells obtained from the patient.
Takakuwa K; Hataya I; Arakawa M; Tamura M; Sekizuka N; Tanaka K
Am J Perinatol; 1997 Nov; 14(10):641-3. PubMed ID: 9605253
[TBL] [Abstract][Full Text] [Related]
8. Identification of an unusual marker chromosome by spectral karyotyping.
Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
[TBL] [Abstract][Full Text] [Related]
9. Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature.
Hastings RJ; Nisbet DL; Waters K; Spencer T; Chitty LS
Prenat Diagn; 1999 May; 19(5):436-45. PubMed ID: 10360512
[TBL] [Abstract][Full Text] [Related]
10. Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
Bryndorf T; Lundsteen C; Lamb A; Christensen B; Philip J
Acta Obstet Gynecol Scand; 2000 Jan; 79(1):8-14. PubMed ID: 10646809
[TBL] [Abstract][Full Text] [Related]
11. [Prenatal diagnosis of two pregnancies with risk of chromosomal disorders].
Cui YX; Huang B; Shi YC; Lu HY; Xia XY; Pan LJ; Huang YF
Zhonghua Nan Ke Xue; 2007 Jul; 13(7):624-7. PubMed ID: 17725307
[TBL] [Abstract][Full Text] [Related]
12. The clinical application of spectral karyotyping (SKY) in the analysis of prenatally diagnosed extra structurally abnormal chromosomes (ESACs).
Yaron Y; Carmon E; Goldstein M; Voskoboinik N; Ochshorn Y; Gelman-Kohan Z; Orr-Urtreger A
Prenat Diagn; 2003 Jan; 23(1):74-9. PubMed ID: 12533818
[TBL] [Abstract][Full Text] [Related]
13. Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.
Iqbal MA; Ramadan S; Ali FA; Kurdi W
Prenat Diagn; 2005 Dec; 25(12):1142-9. PubMed ID: 16240463
[TBL] [Abstract][Full Text] [Related]
14. Characterization of a small supernumerary marker chromosome as r(8) at prenatal diagnosis by MFISH.
Gole LA; Biswas A
Prenat Diagn; 2005 Jan; 25(1):73-8. PubMed ID: 15662692
[TBL] [Abstract][Full Text] [Related]
15. Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up.
Marchina E; Piovani G; Vezzola L; Bellotti D; Cerri V; Groli C; Barlati S
Prenat Diagn; 2003 Dec; 23(12):959-63. PubMed ID: 14663830
[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. 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]
18. Prenatal diagnosis of minute supernumerary marker chromosomes.
Cotter PD; Drexler K; Corley AL; Covert SM; Moland JS; Govberg IJ; Norton ME
Gynecol Obstet Invest; 2005; 60(1):27-38. PubMed ID: 15689640
[TBL] [Abstract][Full Text] [Related]
19. Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis.
Van Opstal D; Eussen HJ; Van Hemel JO; Sachs ES
Prenat Diagn; 1993 Sep; 13(9):825-32. PubMed ID: 8278313
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
