226 related articles for article (PubMed ID: 11031431)
1. [Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations].
Vorsanova SG; Iurov IuB; Solov'ev IV; Demidova IA; Sharonin VO; Male R; Zhiollant M; Beresheva AK; Kolotiĭ AD; Kravets VS; Ruazes Zh
Klin Lab Diagn; 2000 Aug; (8):36-9. PubMed ID: 11031431
[TBL] [Abstract][Full Text] [Related]
2. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
Ulmer R; Pfeiffer RA; Kollert A; Beinder E
Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
[TBL] [Abstract][Full Text] [Related]
3. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours].
Steinborn A; Röddiger S; Born HJ; Baier P; Halberstadt E
Z Geburtshilfe Neonatol; 1996; 200(5):186-90. PubMed ID: 9035828
[TBL] [Abstract][Full Text] [Related]
4. [Development of an original computer program FISHMet: use for molecular cytogenetic diagnosis and genome mapping by fluorescent in situ hybridization (FISH)].
Iurov IuB; Khazatskiĭ IA; Akindinov VA; Dovgilov LV; Kobrinskiĭ BA; Vorsanova SG
Klin Lab Diagn; 2000 Aug; (8):34-6. PubMed ID: 11031430
[TBL] [Abstract][Full Text] [Related]
5. [Molecular cytogenetic pre- and postnatal diagnosis of chromosomal abnormalities].
Vorsanova SG; Iurov IuB
Vestn Ross Akad Med Nauk; 1999; (11):12-5. PubMed ID: 10635746
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Molecular cytogenetic studies of chromosomal abnormalities and disorders in nervous and mental diseases: search for biological markers for diagnosis].
Iurov IuB; Vorsanova SG
Vestn Ross Akad Med Nauk; 2001; (7):26-31. PubMed ID: 11523424
[TBL] [Abstract][Full Text] [Related]
8. Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis.
Knight SJ; Flint J
J Med Genet; 2000 Jun; 37(6):401-9. PubMed ID: 10851249
[TBL] [Abstract][Full Text] [Related]
9. Prenatal cytogenetic abnormalities: correlations of structural rearrangements and ultrasonographically detected fetal anomalies.
Hume RF; Kilmer-Ernst P; Wolfe HM; Ebrahim SA; Treadwell MC; Johnson MP; Evans MI
Am J Obstet Gynecol; 1995 Oct; 173(4):1334-6. PubMed ID: 7485349
[TBL] [Abstract][Full Text] [Related]
10. Results and pitfalls in prenatal cytogenetic diagnosis.
Hsu LY; Dubin EC; Kerenyi T; Hirschhorn K
J Med Genet; 1973 Jun; 10(2):112-9. PubMed ID: 4268389
[TBL] [Abstract][Full Text] [Related]
11. A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities.
Jacobs PA; Matsuura JS; Mayer M; Newlands IM
Clin Genet; 1978 Jan; 13(1):37-60. PubMed ID: 146575
[TBL] [Abstract][Full Text] [Related]
12. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
Iourov IY; Soloviev IV; Vorsanova SG; Monakhov VV; Yurov YB
J Histochem Cytochem; 2005 Mar; 53(3):401-8. PubMed ID: 15750029
[TBL] [Abstract][Full Text] [Related]
13. Inv dup(15) supernumerary marker chromosomes.
Webb T
J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
[No Abstract] [Full Text] [Related]
14. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
[TBL] [Abstract][Full Text] [Related]
15. A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones.
Popp S; Jauch A; Schindler D; Speicher MR; Lengauer C; Donis-Keller H; Riethman HC; Cremer T
Hum Genet; 1993 Dec; 92(6):527-32. PubMed ID: 8262510
[TBL] [Abstract][Full Text] [Related]
16. [Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities].
Romana SP; Gosset P; Elghezal H; Le Lorc'h M; Ozilou C; Lapierre JM; Sanlaville D; Brisset S; Turleau C; Vekemans M
J Gynecol Obstet Biol Reprod (Paris); 2001 Feb; 30(1 Suppl):75-9. PubMed ID: 11240520
[No Abstract] [Full Text] [Related]
17. Traditional and molecular cytogenetics.
Sawyer JR; Johnson MP; Miller OJ
J Reprod Med; 1992 Jun; 37(6):485-98. PubMed ID: 1619601
[TBL] [Abstract][Full Text] [Related]
18. Detection of chromosomal abnormalities using fluorescence in situ hybridization (FISH).
Jobanputra V; Kriplani A; Choudhry VP; Kucheria K
Natl Med J India; 1998; 11(6):259-63. PubMed ID: 10083791
[TBL] [Abstract][Full Text] [Related]
19. Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.
Schmid M; Stary S; Blaicher W; Gollinger M; Husslein P; Streubel B
Prenat Diagn; 2012 Apr; 32(4):376-82. PubMed ID: 22025351
[TBL] [Abstract][Full Text] [Related]
20. [Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique].
Pérez Losada A; Solé F; Woessner S; Florensa L; Besses C; Espinet B; Caballín MR; García Eroles L; Sans-Sabrafén J
Sangre (Barc); 1996 Jun; 41(3):201-9. PubMed ID: 8755208
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]