Showing 1 - 20 results of 24 for search 'QUANTITATIVE METHODS FOR HOSPITALITY RESEARCH', query time: 1.15s Refine Results
  1. 1
    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: “...quantitative fluorescent polymerase chain reaction...”
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    Article
  2. 2
    Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia
    Subjects: “...quantitative fluorescent polymerase chain reaction...”
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  3. 3
    Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review
    “... and methods: A 37-year-old woman underwent amniocentesis at 17 weeks of gestation because of advanced maternal...”
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    Article
  4. 4
    Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review
    “... review of the literature of mosaic trisomy 17 at amniocentesis. Materials and Methods: A 42-year-old...”
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    Article
  5. 5
    Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature review
    “... the literature. Materials and methods: A 37-year-old woman underwent amniocentesis at 20 weeks' gestation because...”
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  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
    “... marker chromosome (sSMC) derived from chromosome 8. Materials and Methods: An 18-year-old female...”
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    Article
  7. 7
    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
    “... marker chromosome (sSMC) derived from chromosome 8. Materials and Methods: A 35-year-old woman underwent...”
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  8. 8
    De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: Prenatal diagnosis and molecular cytogenetic characterization
    “... monosomy 14q (14q32.31 → qter). Materials and Methods: A 33-year-old woman underwent amniocentesis at 20...”
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  9. 9
    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
    “... chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3). Materials, Methods, and Results: A 32...”
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  10. 10
    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
    “... isochromosome 20q at amniocentesis. Materials and methods: A 36-year-old woman underwent amniocentesis at 17...”
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  11. 11
    Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review
    “.... Materials, Methods, and Results: A 34-year-old woman underwent amniocentesis at 16 weeks of gestation...”
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  12. 12
    Trisomy 7 mosaicism at amniocentesis: Interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism
    “...Objective: To present prenatal diagnosis of true trisomy 7 mosaicism. Materials, Methods...”
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    Article
  13. 13
    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
    “...q14 microdeletion associated with tetralogy of Fallot (TOF). Materials and methods...”
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    Article
  14. 14
    Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis
    “... the literature. Materials and Methods: A 34-year-old woman underwent amniocentesis at 17 weeks of gestation...”
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    Article
  15. 15
    Double aneuploidy with Edwards–Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb
    “..., and to review the literature. Materials, Methods, and Results: A 42-year-old woman was referred...”
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    Article
  16. 16
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2
    “... for a small supernumerary marker chromosome (sSMC) derived from ring chromosome 2 [r(2)]. Methods...”
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  17. 17
    Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
    “...Objective: To present prenatal diagnosis of mosaic trisomy 2. Materials and Methods: A 29-year-old...”
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    Article
  18. 18
    First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination
    “...) associated with dizygotic twin pregnancy conceived by intrauterine insemination. Materials and methods: A 32...”
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  19. 19
    Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister–Killian syndrome
    “... syndrome (PKS). Materials and methods: A 37-year-old woman underwent amniocentesis at 18 weeks of gestation...”
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  20. 20
    Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15)
    “... (sSMC) at amniocentesis associated with concomitant microduplication of 8q22.1. Materials and methods: A...”
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