Showing 1 - 14 results of 14 for search '"fluorescent in situ hybridization"', query time: 0.39s Refine Results
  1. 1
    Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements
    “... dysmorphism. Postnatal analysis of fetal tissues using spectral karyotyping, fluorescence in situ...”
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    Article
  2. 2
    Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis
    “... in situ hybridization (FISH), and quantitative fluorescent polymerase chain reaction (QF-PCR) were...”
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    Article
  3. 3
    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
  4. 4
    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
  5. 5
    Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family
    “.... Array comparative genomic hybridization (aCGH) and fluorescence in situ hybridization were applied...”
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    Article
  6. 6
    Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry
    “... duplication at chromosome 14q31.3-q32.12. Results of a fluorescence in situ hybridization analysis showed a...”
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    Article
  7. 7
    Trisomy 7 mosaicism at amniocentesis: Interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism
    “... in the maternal allele. Interphase fluorescence in situ hybridization (FISH) on uncultured amniocytes revealed...”
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    Article
  8. 8
    Prenatal diagnosis of mosaic tetrasomy 18p
    “... supernumerary marker chromosome derived from isochromosome 18p, by interphase fluorescence in situ hybridization...”
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    Article
  9. 9
    Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry
    “... paternal origin of the duplication. Results of fluorescence in situ hybridization analysis showed a direct...”
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    Article
  10. 10
    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
  11. 11
    Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis
    “... in situ hybridization (FISH) and quantitative fluorescent polymerase chain reaction (QF-PCR) were applied...”
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    Article
  12. 12
    Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion
    “.... Fluorescence in situ hybridization study showed an unbalanced reciprocal translocation between chromosomes 4...”
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    Article
  13. 13
    Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
    “.... Interphase fluorescence in situ hybridization (FISH), array comparative genomic hybridization (aCGH...”
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    Article
  14. 14
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2
    “... (aCGH), interphase fluorescence in situ hybridization (FISH) and quantitative fluorescent polymerase...”
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    Article
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