Showing 1 - 20 results of 20 for search '"fluorescent in situ hybridization"', query time: 0.24s Refine Results
  1. 1
    Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister–Killian syndrome
    “... in situ hybridization (FISH) analysis was performed using uncultured amniocytes and cultured stimulated...”
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    Article
  2. 2
    Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis
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    Article
  3. 3
    Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis
    Subjects: “...interphase fluorescence in situ hybridization...”
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    Article
  4. 4
    Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality
    “... genetic analysis. Results: At repeat amniocentesis, interphase fluorescence in situ hybridization analysis...”
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    Article
  5. 5
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11
    “...) using 24-color SKY probes and fluorescence in situ hybridization (FISH) using a whole chromosome paint...”
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    Article
  6. 6
    Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction
    “... analysis and metaphase fluorescence in situ hybridization (FISH) were applied on cord blood lymphocytes...”
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    Article
  7. 7
    Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses
    “... amniocytes revealed no genomic imbalance in chromosome 9. However, interphase fluorescence in situ...”
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    Article
  8. 8
    Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome
    “... with 40% (4/10) mosaicism for trisomy 12. Interphase fluorescence in situ hybridization (FISH) on 112...”
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    Article
  9. 9
    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
  10. 10
    Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review
    “... repeat amniocentesis at 20 weeks of gestation. Interphase fluorescence in situ hybridization (FISH...”
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    Article
  11. 11
    Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis
    “..., interphase fluorescence in situ hybridization (FISH), array comparative genomic hybridization (aCGH...”
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    Article
  12. 12
    Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
    “... of gestation. Interphase fluorescence in situ hybridization (FISH) analysis showed four 18p11.22-specific probe...”
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    Article
  13. 13
    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
  14. 14
    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
  15. 15
    Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysis
    “... fluorescence in situ hybridization (FISH) analysis on uncultured amniocytes using a 2q11.1-specific probe RP11...”
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    Article
  16. 16
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16
    “... RPGRIP1L, FTO, SLC6A2, BBS2 and CDH1. Interphase fluorescence in situ hybridization (FISH) analysis...”
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    Article
  17. 17
    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
  18. 18
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
    “... karyotyping (SKY), fluorescence in situ hybridization (FISH), and array comparative genomic hybridization...”
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    Article
  19. 19
    Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15)
    “... comparative genomic hybridization (aCGH), fluorescence in situ hybridization (FISH), quantitative fluorescent...”
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    Article
  20. 20
    Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9
    “... normal psychomotor and growth development. Cytogenetic analysis, metaphase fluorescence in situ...”
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    Article
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