Showing 1 - 15 results of 15 for search '"fluorescent in situ hybridization"', query time: 0.30s 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
    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
  3. 3
    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
  4. 4
    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
  5. 5
    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
  6. 6
    Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats
    “..., psu idic(8)(p23.3)[37]/45,XY,-8,psu idic(8)(p23.3)[13]. Fluorescence in situ hybridization studies...”
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    Article
  7. 7
    Prenatal Diagnosis of mos45,X/46,X,+mar in a Fetus With Normal Male External Genitalia and a Literature Review
    “..., the addition of fluorescence in situ hybridization and molecular analysis to the conventional cytogenetic...”
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    Article
  8. 8
    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
  9. 9
    Ventriculomegaly, Intrauterine Growth Restriction, and Congenital Heart Defects as Salient Prenatal Sonographic Findings of Miller-Dieker Lissencephaly Syndrome Associated With Monosomy 17p (17p13.2 → pter) in a Fetus
    “... by rapid fluorescence in situ hybridization analysis. Cytogenetic analysis of the cord blood revealed a 46...”
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    Article
  10. 10
    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
  11. 11
    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
  12. 12
    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
  13. 13
    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
  14. 14
    Mosaic Trisomy 7 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses
    “... hypopigmented skin and inguinal hernia, but showed normal growth and mental development. Fluorescence in situ...”
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    Article
  15. 15
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
    “... karyotyping (SKY), fluorescence in situ hybridization (FISH), and array comparative genomic hybridization...”
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    Article
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