Showing 1 - 20 results of 92 for search '"fluorescent in situ hybridization"', query time: 1.65s Refine Results
  1. 1
    Interphase fluorescence in situ hybridization assisting in prenatal counseling for amniocentesis karyotyping-detected fetal mosaicism
    Subjects: “...interphase fluorescence in situ hybridization...”
    Get full text
    Article
  2. 2
    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...”
    Get full text
    Article
  3. 3
    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...”
    Get full text
    Article
  4. 4
    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...”
    Get full text
    Article
  5. 5
    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...”
    Get full text
    Article
  6. 6
    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
    Get full text
    Article
  7. 7
    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...”
    Get full text
    Article
  8. 8
    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...”
    Get full text
    Article
  9. 9
    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...”
    Get full text
    Article
  10. 10
    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...”
    Get full text
    Article
  11. 11
    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...”
    Get full text
    Article
  12. 12
    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...”
    Get full text
    Article
  13. 13
    Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature review
    “.... Array comparative genomic hybridization, interphase fluorescence in situ hybridization, and quantitative...”
    Get full text
    Article
  14. 14
    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...”
    Get full text
    Article
  15. 15
    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...”
    Get full text
    Article
  16. 16
    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...”
    Get full text
    Article
  17. 17
    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...”
    Get full text
    Article
  18. 18
    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...”
    Get full text
    Article
  19. 19
    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...”
    Get full text
    Article
  20. 20
    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...”
    Get full text
    Article
Search Tools: Get RSS Feed — Email this Search