Showing 1 - 20 results of 26 for search '"fluorescent in situ hybridization"', query time: 1.98s Refine Results
  1. 1
    Inv dup del(9p): Prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization
    “.... Fluorescence in situ hybridization analysis using bacterial artificial chromosome clone probes specific for 9p...”
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    Article
  2. 2
    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
  3. 3
    Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization
    Subjects: “...fluorescence in situ hybridization...”
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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
    A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization
    “... (PGD) with blastomere biopsy and fluorescent in-situ hybridization (FISH) has been used to select...”
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    Article
  6. 6
    Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review
    “... of mosaic trisomy 8, follow-up investigations should include interphase fluorescence in situ hybridization...”
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    Article
  7. 7
    Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly
    “... from a translocation of chromosomes 7 and 13. Fluorescence in situ hybridization using subtelomeric...”
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    Article
  8. 8
    Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly
    “... of 18q22.3-q23. Metaphase fluorescence in situ hybridization study showed the absence of an 18q12.1...”
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    Article
  9. 9
    Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 18 and Associated With a Reciprocal Translocation Involving Chromosomes 17 And 18
    “... karyotyping, fluorescence in situ hybridization, multicolor-fluorescence in situ hybridization, or array...”
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    Article
  10. 10
    De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure
    “... analysis revealed a karyotype of 46,X,dup(X)(q22.1q24). Fluorescence in situ hybridization determined a...”
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    Article
  11. 11
    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
  12. 12
    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
  13. 13
    Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3)
    “... from 15q26.2 to 15q26.3 encompassing the IGF1R gene. Fluorescence in situ hybridization analysis using...”
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    Article
  14. 14
    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
  15. 15
    Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia
    “... fluorescence in situ hybridization revealed diploidy and array comparative genomic hybridization revealed...”
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    Article
  16. 16
    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
  17. 17
    Prenatal diagnosis of mosaic tetrasomy 18p
    “... supernumerary marker chromosome derived from isochromosome 18p, by interphase fluorescence in situ hybridization...”
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    Article
  18. 18
    A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
    “... chromosome 9, or der(9). Parental karyotypes were normal. Spectral karyotyping (SKY) and fluorescence in situ...”
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    Article
  19. 19
    Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings
    “..., fluorescence in situ hybridization and array comparative genomic hybridization are useful for the prenatal...”
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    Article
  20. 20
    Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy
    “... (aCGH) and interphase fluorescence in situ hybridization (FISH) were applied in the uncultured...”
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    Article
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