Showing 1 - 12 results of 12 for search '"fluorescent in situ hybridization"', query time: 1.68s 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
    Prenatal diagnosis of partial monosomy 21q (21q22.1→qter) associated with intrauterine growth restriction and corpus callosum dysgenesis
    “.... The interphase fluorescence in situ hybridization (FISH) analysis on amniocytes revealed monosomy 21, while...”
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    Article
  3. 3
    Species and sex comparisons of karyotype and genome size in two <em>Kurixalus tree</em> frogs (Anura, Rhacophoridae)
    by Shun-Ping Chang, Gwo-Chin Ma, Ming Chen, Sheng-Hai Wu
    Published 2017-12-01
    “...-banding and silver-staining techniques, fluorescence in situ hybridization (FISH), and flow cytometry...”
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    Article
  4. 4
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review
    “... encompassing the genes of LIPI, ABCC13 and NRIP1. Metaphase 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
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2
    “.... Spectral karyotyping analysis failed to identify the sSMC. Metaphase fluorescence in situ hybridization...”
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    Article
  7. 7
    Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray
    “... karyotype of 47,XY,+mar[4]/46,XY[16]. Spectral karyotyping and metaphase fluorescence in situ hybridization...”
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    Article
  8. 8
    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
  9. 9
    Low-level mosaicism for trisomy 16 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome
    “...) mosaicism for trisomy 16. Interphase fluorescence in situ hybridization (FISH) analysis detected trisomy 16...”
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    Article
  10. 10
    Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay
    “... (aCGH) and metaphase fluorescence in situ hybridization (FISH) were applied on cultured amniocytes...”
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    Article
  11. 11
    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
  12. 12
    Genomic studies of the sex determination mode in two Kurixalus species (K. eiffingeri and K. idiootocus)
    by Shun-Ping Chang, 張舜評
    Published 2018
    “..., fluorescence in situ hybridization (FISH), and flow cytometry in two representatives of Kurixalus (K...”
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