Showing 1 - 20 results of 26 for search '"fluorescent in situ hybridization"', query time: 0.61s Refine Results
  1. 1
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia
    “... for chromosome 2. Metaphase fluorescence in situ hybridization analysis confirmed an sSMC derived from chromosome...”
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    Article
  2. 2
    Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a pregnancy with a favorable outcome
    “... was performed at 19 weeks of gestation. Interphase fluorescence in situ hybridization (FISH) was applied...”
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    Article
  3. 3
    Prenatal diagnosis of mosaicism for trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome
    “... in 40/40 lymphocytes. Postnatal interphase fluorescence in situ hybridization (FISH) analysis on buccal...”
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    Article
  4. 4
    Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome
    “... weeks of gestation. Interphase fluorescence in situ hybridization (FISH) was applied on the uncultured...”
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    Article
  5. 5
    Low-level mosaic trisomy 13 at amniocentesis associated with a favorable outcome in a pregnancy
    “... fluorescence in situ hybridization (FISH) analysis revealed no trisomy 13 signals in 100/100 buccal mucosal...”
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    Article
  6. 6
    Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion
    “... a karyotype of 46,XY. Postnatal urinary cells analysis by interphase fluorescence in situ...”
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    Article
  7. 7
    Prenatal diagnosis of a familial Y long-arm and chromosome 15 short-arm translocation inherited from a mother carrier
    “... preparations and metaphase fluorescence in situ hybridization analysis using a Yq12-specific probe showed a...”
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    Article
  8. 8
    Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion
    “.... Metaphase fluorescence in situ hybridization (FISH) analysis of the umbilical cord fibroblasts confirmed a...”
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    Article
  9. 9
    Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome
    “... hybridization (aCGH) analysis and a mosaic level of 14.3% (15/105 cells) in interphase fluorescence in situ...”
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    Article
  10. 10
    Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcome
    “... normal. Repeat amniocentesis was performed at 21 weeks of gestation. Interphase fluorescence in situ...”
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    Article
  11. 11
    Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy
    “... of maternal origin and maternal UPD 5. aCGH and interphase fluorescence in situ hybridization (FISH...”
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    Article
  12. 12
    Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects
    “... in situ hybridization analysis confirmed a 1q41 deletion. Conclusion: Genetic counseling of the parents...”
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    Article
  13. 13
    Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus
    “... amniocytes revealed 22.4% mosaicism (26/116 cells) for trisomy 16 on interphase fluorescence in situ...”
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    Article
  14. 14
    Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome
    “... uniparental heterodisomy 21 in the baby. Interphase fluorescence in situ hybridization analysis on buccal...”
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    Article
  15. 15
    Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis
    “... in interphase fluorescence in situ hybridization (FISH) analysis, and no uniparental disomy (UPD) 7 and no UPD...”
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    Article
  16. 16
    Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome
    “... blood. Simultaneous molecular genetic analysis such as interphase fluorescence in situ hybridization...”
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    Article
  17. 17
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3
    “...13B, NSUN3 and EPHA6. Metaphase fluorescence in situ hybridization (FISH) analysis confirmed 30% (6...”
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    Article
  18. 18
    Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization
    “... of 10p15.3. Fluorescence in situ hybridization (FISH) analysis of the cord blood confirmed inverted...”
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    Article
  19. 19
    Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis
    “... was referred for repeat amniocentesis. aCGH, interphase fluorescence in situ hybridization (FISH), quantitative...”
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    Article
  20. 20
    Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review
    “... hybridization (aCGH), interphase fluorescence in situ hybridization (FISH) and quantitative fluorescent...”
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    Article
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