Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders von Tropeano, Maria, Ahn, Joo Wook, Dobson, Richard J B, Breen, Gerome, Rucker, James, Dixit, Abhishek, Pal, Deb K, McGuffin, Peter, Farmer, Anne, White, Peter S, Andrieux, Joris, Vassos, Evangelos, Ogilvie, Caroline Mackie, Curran, Sarah, Collier, David A

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Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryos von Mackie Ogilvie, Caroline, Scriven, Paul N

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Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance von Ahn, Joo Wook, Mann, Kathy, Walsh, Sally, Shehab, Marwa, Hoang, Sarah, Docherty, Zoe, Mohammed, Shehla, Mackie Ogilvie, Caroline

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Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis von Mann, Kathy, Fox, Susan P, Abbs, Stephen J, Yau, Shu Ching, Scriven, Paul N, Docherty, Zoe, Ogilvie, Caroline Mackie

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

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Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues? von Pichert, Gabriella, Mohammed, Shehla Nilofer, Ahn, Joo Wook, Ogilvie, Caroline Mackie, Izatt, Louise

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Array comparative genomic hybridization (array CGH) for detection of genomic copy number variants von Ahn, Joo Wook, Coldwell, Michael, Bint, Susan, Mackie Ogilvie, Caroline

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Preimplantation genetic diagnosis for a carrier of a Y;autosome translocation resulting in a healthy male offspring von Mackie Ogilvie, Caroline, D.Phil, Watson, Sally, M.Sc, Braude, Peter, Ph.D, Pickering, Susan, Ph.D, Scriven, Paul N., Ph.D

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Reply: Embryo selection and IVF von Scriven, Paul N., Mackie Ogilvie, Caroline, Khalaf, Yacoub

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QF-PCR: application, overview and review of the literature von Mann, Kathy, Ogilvie, Caroline Mackie

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The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testing von Ogilvie, Caroline Mackie, Lashwood, Alison, Chitty, Lyn, Waters, Jonathan J., Scriven, Paul N., Flinter, Frances

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Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12 qh involve deletion, duplication and triplication of large tracts of segmentally duplicated perice... von WILLATT, Lionel R, BARBER, John C. K, CLARKSON, Amanda, SIMONIC, Ingrid, RAYMOND, F. Lucy, DOCHERTY, Zoe, MACKIE OGILVIE, Caroline

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Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis von Donaghue, Celia, Mann, Kathy, Docherty, Zoe, Mackie Ogilvie, Caroline

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The copy number variant involving part of the α7 nicotinic receptor gene contains a polymorphic inversion von Flomen, Rachel H, Davies, Angela F, Di Forti, Marta, Cascia, Caterina La, Mackie-Ogilvie, Caroline, Murray, Robin, Makoff, Andrew J

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Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this r... von Male, Alison, Davies, Angela, Bergbaum, Anne, Keeling, Jean, FitzPatrick, David, Mackie Ogilvie, Caroline, Berg, Jonathan

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Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping von Stojilkovic-Mikic, Taita, Mann, Kathy, Docherty, Zoe, Mackie Ogilvie, Caroline

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Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis von Ahn, Joo Wook, Mann, Kathy, Docherty, Zoe, Mackie Ogilvie, Caroline

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Multiple pregnancy, fetal reduction and selective termination von Ogilvie, Caroline Mackie

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Velopharyngeal incompetence and chromosome 22q11 deletion von Boorman, John G, Varma, Sanjay, Ogilvie, Caroline Mackie

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Preimplantation genetic diagnosis for monogenic diseases: overview and emerging issues von Renwick, Pamela, Ogilvie, Caroline Mackie

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