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Array comparative genomic hybridisation of 52 subjects with a Smith–Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay
Williams, Stephen R, Girirajan, Santhosh, Tegay, David, Nowak, Norma, Hatchwell, Eli, Elsea, Sarah H
Published in Journal of medical genetics (01.04.2010)
Published in Journal of medical genetics (01.04.2010)
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Array comparative genomic hybridisation on first polar bodies suggests that non-disjunction is not the predominant mechanism leading to aneuploidy in humans
Gabriel, A S, Thornhill, A R, Ottolini, C S, Gordon, A, Brown, A P C, Taylor, J, Bennett, K, Handyside, A, Griffin, D K
Published in Journal of medical genetics (01.07.2011)
Published in Journal of medical genetics (01.07.2011)
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High resolution comparative genomic hybridisation in clinical cytogenetics
Kirchhoff, Maria, Rose, Hanne, Lundsteen, Claes
Published in Journal of medical genetics (01.11.2001)
Published in Journal of medical genetics (01.11.2001)
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Preimplantation genetic diagnosis and screening by array comparative genomic hybridisation: experience of more than 100 cases in a single centre
Chow, Judy FC, Yeung, William SB, Lee, Vivian CY, Lau, Estella YL, Ho, PC, Ng, Ernest HY
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01.04.2017)
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01.04.2017)
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Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions
El-Hattab, Ayman W, Fang, Ping, Jin, Weihong, Hughes, Jeffrey R, Gibson, James B, Patel, Gayle S, Grange, Dorothy K, Manwaring, Linda P, Patel, Ankita, Stankiewicz, Pawel, Cheung, Sau Wai
Published in Journal of medical genetics (01.12.2011)
Published in Journal of medical genetics (01.12.2011)
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Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1
Rajcan-Separovic, E, Harvard, C, Liu, X, McGillivray, B, Hall, J G, Qiao, Y, Hurlburt, J, Hildebrand, J, Mickelson, E C R, Holden, J J A, Lewis, M E S
Published in Journal of medical genetics (01.04.2007)
Published in Journal of medical genetics (01.04.2007)
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Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1
Slavotinek, A, Lee, S S, Davis, R, Shrit, A, Leppig, K A, Rhim, J, Jasnosz, K, Albertson, D, Pinkel, D
Published in Journal of medical genetics (01.09.2005)
Published in Journal of medical genetics (01.09.2005)
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An atypical deletion of the Williams–Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism
Edelmann, Lisa, Prosnitz, Aaron, Pardo, Sherly, Bhatt, Jahnavi, Cohen, Ninette, Lauriat, Tara, Ouchanov, Leonid, González, Patricia J, Manghi, Elina R, Bondy, Pamela, Esquivel, Marcela, Monge, Silvia, Delgado, Marietha F, Splendore, Alessandra, Francke, Uta, Burton, Barbara K, McInnes, L Alison
Published in Journal of medical genetics (01.02.2007)
Published in Journal of medical genetics (01.02.2007)
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HER2 gene amplification in patients with breast cancer with equivocal IHC results
Meijer, Sybren L, Wesseling, Jelle, Smit, Vincent T, Nederlof, Petra M, Hooijer, Gerrit K J, Ruijter, Henrique, Arends, Jan Willem, Kliffen, Mike, van Gorp, Joost M, Sterk, Lotus, van de Vijver, Marc J
Published in Journal of clinical pathology (01.12.2011)
Published in Journal of clinical pathology (01.12.2011)
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Limited tissue fixation times and whole genomic amplification do not impact array CGH profiles
Ghazani, A A, Arneson, N C R, Warren, K, Done, S J
Published in Journal of clinical pathology (01.03.2006)
Published in Journal of clinical pathology (01.03.2006)
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Published in European journal of haematology
(01.06.2003)
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Published in European journal of haematology
(01.06.2003)
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Comparative genomic hybridization on microarray (a-CGH) in olfactory neuroblastoma: Analysis of ten cases and review of the literature
Valli, Roberto, De Bernardi, Francesca, Frattini, Annalisa, Volpi, Luca, Bignami, Maurizio, Facchetti, Fabio, Pasquali, Francesco, Castelnuovo, Paolo, Maserati, Emanuela
Published in Genes chromosomes & cancer (01.12.2015)
Published in Genes chromosomes & cancer (01.12.2015)
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Molecular Karyotyping of Human Single Sperm by Array- Comparative Genomic Hybridization
Patassini, Cristina, Garolla, Andrea, Bottacin, Alberto, Menegazzo, Massimo, Speltra, Elena, Foresta, Carlo, Ferlin, Alberto
Published in PloS one (02.04.2013)
Published in PloS one (02.04.2013)
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Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility
Costantini, Alice, Skarp, Sini, Kämpe, Anders, Mäkitie, Riikka E., Pettersson, Maria, Männikkö, Minna, Jiao, Hong, Taylan, Fulya, Lindstrand, Anna, Mäkitie, Outi
Published in Frontiers in endocrinology (Lausanne) (10.07.2018)
Published in Frontiers in endocrinology (Lausanne) (10.07.2018)
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Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
Osoegawa, K, Vessere, G M, Utami, K H, Mansilla, M A, Johnson, M K, Riley, B M, L’Heureux, J, Pfundt, R, Staaf, J, van der Vliet, W A, Lidral, A C, Schoenmakers, E F P M, Borg, A, Schutte, B C, Lammer, E J, Murray, J C, de Jong, P J
Published in Journal of medical genetics (01.02.2008)
Published in Journal of medical genetics (01.02.2008)
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