Rezultati pretrage - Bint, Susan

  • Prikaz rezultata 1 – 6 od 6
Detaljiziraj rezultate
  1. 1
    Multicolor banding remains an important adjunct to array CGH and conventional karyotyping

    Multicolor banding remains an important adjunct to array CGH and conventional karyotyping od Bint, Susan M, Davies, Angela F, Ogilvie, Caroline Mackie

    Izdano 2013
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  2. 2
    Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

    Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants od Ahn, Joo Wook, Coldwell, Michael, Bint, Susan, Mackie Ogilvie, Caroline

    Izdano 2015
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  3. 3
    Meiotic outcomes of three-way translocations ascertained in cleavage-stage embryos: refinement of reproductive risks and implications for PGD

    Meiotic outcomes of three-way translocations ascertained in cleavage-stage embryos: refinement of reproductive risks and implications for PGD od Scriven, Paul N, Bint, Susan M, Davies, Angela F, Ogilvie, Caroline Mackie

    Izdano 2014
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  4. 4
    Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients

    Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients od Ahn, Joo Wook, Bint, Susan, Bergbaum, Anne, Mann, Kathy, Hall, Richard P, Ogilvie, Caroline Mackie

    Izdano 2013
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  5. 5
    A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings

    A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings od Ahn, Joo Wook, Bint, Susan, Irving, Melita D., Kyle, Phillipa M., Akolekar, Ranjit, Mohammed, Shehla N., Mackie Ogilvie, Caroline

    Izdano 2014
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  6. 6
    Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity

    Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity od Cottrell, Emily, Cabrera, Claudia P, Ishida, Miho, Chatterjee, Sumana, Greening, James, Wright, Neil, Bossowski, Artur, Dunkel, Leo, Deeb, Asma, Basiri, Iman Al, Rose, Stephen J, Mason, Avril, Bint, Susan, Ahn, Joo Wook, Hwa, Vivian, Metherell, Louise A, Moore, Gudrun E, Storr, Helen L

    Izdano 2020
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