Showing 1 - 20 results of 61 for search '"fluorescent in situ hybridization"', query time: 3.20s Refine Results
  1. 1
    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
  2. 2
    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
  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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  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
    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
    Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability
    “...11.21::). Metaphase fluorescence in situ hybridization analysis using the probes of RP11-754D24 (8p11.21...”
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    Article
  7. 7
    Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature review
    “.... Array comparative genomic hybridization, interphase fluorescence in situ hybridization, and quantitative...”
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    Article
  8. 8
    Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities
    “... comparative genomic hybridization and metaphase fluorescence in situ hybridization analyses were performed...”
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    Article
  9. 9
    Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect
    “... LINGO1, MTHFS, KIF7 and CHD2. Metaphase fluorescence in situ hybridization analysis using 15q25.1...”
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    Article
  10. 10
    Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2–q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome
    “... hybridization (aCGH) was performed on uncultured amniocytes and parental blood. Metaphase fluorescence in situ...”
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    Article
  11. 11
    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
  12. 12
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia
    “... for chromosome 2. Metaphase fluorescence in situ hybridization analysis confirmed an sSMC derived from chromosome...”
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    Article
  13. 13
    Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a pregnancy with a favorable outcome
    “... was performed at 19 weeks of gestation. Interphase fluorescence in situ hybridization (FISH) was applied...”
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    Article
  14. 14
    Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1
    “... in situ hybridization analysis on cultured amniocytes confirmed an 18q proximal interstitial deletion...”
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    Article
  15. 15
    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
  16. 16
    Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion
    “... a karyotype of 46,XY. Postnatal urinary cells analysis by interphase fluorescence in situ...”
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    Article
  17. 17
    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
  18. 18
    Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
    “.... Interphase fluorescence in situ hybridization (FISH) analysis on uncultured amniocytes revealed a mosaic...”
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    Article
  19. 19
    Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot
    “... hybridization (aCGH) was performed on uncultured amniocytes and parental bloods. Metaphase fluorescence in situ...”
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    Article
  20. 20
    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
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