A de novo 2.3 Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl von Belengeanu, V, Gamage, T H, Farcas, S, Stoian, M, Andreescu, N, Belengeanu, A, Frengen, E, Misceo, D

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Increasing the resolution of the comet assay using fluorescent in situ hybridization—a review von Shaposhnikov, Sergey, Frengen, Eirik, Collins, Andrew R.

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1.5Mb deletion of chromosome 4p16.3 associated with postnatal growth delay, psychomotor impairment, epilepsy, impulsive behavior and asynchronous skeletal development von Misceo, D., Barøy, T., Helle, J.R., Braaten, Ø., Fannemel, M., Frengen, E.

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Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay von Pedurupillay, C.R.J., Misceo, D., Gamage, T.H., Dissanayake, V.H.W., Frengen, E.

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SCA27 caused by a chromosome translocation: further delineation of the phenotype von Misceo, D., Fannemel, M., Barøy, T., Roberto, R., Tvedt, B., Jæger, T., Bryn, V., Strømme, P., Frengen, E.

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A translocation between Xq21.33 and 22q13.33 causes an intragenic SHANK3 deletion in a woman with Phelan–McDermid syndrome and hypergonadotropic hypogonadism von Misceo, D., Rødningen, O.K., Barøy, T., Sorte, H., Mellembakken, J.R., Strømme, P., Fannemel, M., Frengen, E.

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Mutated Thyroid Hormone Transporter OATP1C1 Associates with Severe Brain Hypometabolism and Juvenile Neurodegeneration von Strømme, Petter, Groeneweg, Stefan, Lima de Souza, Elaine C., Zevenbergen, Chantal, Torgersbråten, Anette, Holmgren, Asbjørn, Gurcan, Ebrar, Meima, Marcel E., Peeters, Robin P., Visser, W. Edward, Høneren Johansson, Linda, Babovic, Almira, Zetterberg, Henrik, Heuer, Heike, Frengen, Eirik, Misceo, Doriana, Visser, Theo J.

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STIM1 R304W causes muscle degeneration and impaired platelet activation in mice von Gamage, Thilini H., Gunnes, Gjermund, Lee, Robert Hugh, Louch, William Edward, Holmgren, Asbjørn, Bruton, Joseph D., Lengle, Emma, Kolstad, Terje R. Selnes, Revold, Tobias, Amundsen, Silja Svanstrøm, Dalen, Knut Tomas, Holme, Pål Andre, Tjønnfjord, Geir Erland, Christensen, Geir, Westerblad, Håkan, Klungland, Arne, Bergmeier, Wolfgang, Misceo, Doriana, Frengen, Eirik

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A de novo 2.3Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl von Belengeanu, V., Gamage, T.H., Farcas, S., Stoian, M., Andreescu, N., Belengeanu, A., Frengen, E., Misceo, D.

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Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype von Skauli, Nadia, Wallace, Sean, Chiang, Samuel C C, Barøy, Tuva, Holmgren, Asbjørn, Stray-Pedersen, Asbjørg, Bryceson, Yenan T, Strømme, Petter, Frengen, Eirik, Misceo, Doriana

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A bacterial artificial chromosome library for sequencing the complete human genome von Osoegawa, K, Mammoser, A G, Wu, C, Frengen, E, Zeng, C, Catanese, J J, de Jong, P J

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Organization, chromosomal localization and promoter analysis of the gene encoding human acidic fibroblast growth factor intracellular binding protein von Kolpakova, E, Frengen, E, Stokke, T, Olsnes, S

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A highly redundant BAC library of Atlantic salmon (Salmo salar): an important tool for salmon projects von Thorsen, Jim, Zhu, Baoli, Frengen, Eirik, Osoegawa, Kazutoyo, de Jong, Pieter J, Koop, Ben F, Davidson, William S, Høyheim, Bjørn

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Alternative transcripts of the candidate tumor suppressor gene, WWOX, are expressed at high levels in human breast tumors von DRIOUCH, Keltouma, PRYDZ, Hans, MONESE, Rossana, JOHANSEN, Henning, LIDEREAU, Rosette, FRENGEN, Eirik

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Bacterial artificial chromosome libraries for mouse sequencing and functional analysis von Osoegawa, K, Tateno, M, Woon, P Y, Frengen, E, Mammoser, A G, Catanese, J J, Hayashizaki, Y, de Jong, P J

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An Improved Approach for Construction of Bacterial Artificial Chromosome Libraries von Osoegawa, Kazutoyo, Woon, Peng Yeong, Zhao, Baohui, Frengen, Eirik, Tateno, Minako, Catanese, Joseph J., de Jong, Pieter J.

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Alternative transcripts of the candidate tumor suppressor gene, WWOX, are expressed at high levels in human breast tumors von Driouch, K, Prydz, H, Monese, R, Johansen, H, Lidereau, R, Frengen, E

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Altered NDRG1 expression in breast cell lines influences apoptosis von Gjernes, E, Askautrud, H.A, Størvold, G.L, Ross, D.T, Børresen-Dale, A.L, Perou, C.M, Frengen, E

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Construction of Bacterial Artificial Chromosome (BAC/PAC) Libraries von Osoegawa, Kazutoyo, Jong, Pieter J., Frengen, Eirik, Ioannou, Panayiotis A.

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Cloning and Characterization of MDDX28, a Putative DEAD-box Helicase with Mitochondrial and Nuclear Localization von Valgardsdottir, R, Brede, G, Eide, L G, Frengen, E, Prydz, H

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