Showing 1 - 17 results of 17 for search '"fluorescent in situ hybridization"', query time: 0.60s Refine Results
  1. 1
    Prenatal Diagnosis and Genetic Analysis of a Fetus with 47,XX, +21/46,XX Mosaicism and XX/XY Chimerism
    “... findings of both fetuses were normal. Fluorescence in situ hybridization identified three cell lines...”
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    Article
  2. 2
    Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
    “... 22 low copy number repeat 22-A–C. Metaphase fluorescence in situ hybridization on lymphocyte in cord...”
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    Article
  3. 3
    Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion
    “... in situ hybridization analysis revealed a duplication of terminal 10p and a deletion of terminal 10q...”
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    Article
  4. 4
    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
  5. 5
    Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
    “... karyotype 46,XY. Metaphase fluorescence in situ hybridization (FISH) analysis on cultured amniocytes...”
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    Article
  6. 6
    Prenatal diagnosis of mosaic tetrasomy 18p
    “... supernumerary marker chromosome derived from isochromosome 18p, by interphase fluorescence in situ hybridization...”
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    Article
  7. 7
    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
  8. 8
    Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities
    “... but not PAFAH1B1. Metaphase fluorescence in situ hybridization analysis using the 17p13.3-specific probe of RP11...”
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    Article
  9. 9
    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
  10. 10
    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
  11. 11
    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
  12. 12
    Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 8
    “... amplification (MLPA), fluorescence in situ hybridization (FISH), spectral karyotyping (SKY) and array...”
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    Article
  13. 13
    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
  14. 14
    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
  15. 15
    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
  16. 16
    Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes
    “... at birth revealed no genomic imbalance. Interphase fluorescence in situ hybridization analysis on buccal...”
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    Article
  17. 17
    Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2)dup(X)(q25q22.3)/ 46,XX at amniocentesis in a pregnancy with a favorable outcome
    “... fluorescence in situ hybridization (FISH) analysis on buccal mucosal cells showed Xq duplication signals...”
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    Article
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