Corrigenda (English)
In:
Human molecular genetics
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8
, 9
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1817-
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1999
- Article (Journal) / Electronic Resource
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Title:Corrigenda
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Published in:Human molecular genetics ; 8, 9 ; 1817-
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Publisher:
- New search for: Oxford University Press
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Publication date:1999-09-01
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 8, Issue 9
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1589
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Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in -sarcoglycan-deficient miceAraishi, K. / Sasaoka, T. / Imamura, M. / Noguchi, S. / Hama, H. / Wakabayashi, E. / Yoshida, M. / Hori, T. / Ozawa, E. et al. | 1999
- 1589
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Loss of the Sarcoglycan Complex and Sarcospan Leads to Muscular Dystrophy in {beta}-Sarcoglycan-Deficient MiceAraishi, Kenji / Sasaoka, Toshikuni / Imamura, Michihiro / Noguchi, Satoru / Hama, Hiroshi / Wakabayashi, Eriko / Yoshida, Mikiharu / Hori, Tetsuro / Ozawa, Eijiro et al. | 1999
- 1599
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Doublecortin, a Stabilizer of MicrotubulesHoresh, David / Sapir, Tamar / Francis, Fiona / Grayer Wolf, Sharon / Caspi, Michal / Elbaum, Michael / Chelly, Jamel / Reiner, Orly et al. | 1999
- 1611
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Spectrum of novel ATP2A2 mutations in patients with Darier's diseaseSakuntabhai, Anavaj / Burge, Susan / Monk, Sarah / Hovnanian, Alain et al. | 1999
- 1621
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ATP2A2 Mutations in Darier's Disease: Variant Cutaneous Phenotypes Are Associated with Missense Mutations, But Neuropsychiatry Features Are Independent of Mutation ClassRuiz-Perez, Victor L. / Carter, Simon A. / Healy, Eugene / Todd, Carole / Rees, Jonathan L. / Steijlen, Peter M. / Carmichael, Andrew J. / Lewis, Helen M. / Hohl, D. / Itin, Peter et al. | 1999
- 1621
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ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classRuiz-Perez, V. L. / Carter, S. A. / Healy, E. / Todd, C. / Rees, J. L. / Steijlen, P. M. / Carmichael, A. J. / Lewis, H. M. / Hohl, D. / Itin, P. et al. | 1999
- 1631
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ATP2A2 Mutations in Darier's Disease and Their Relationship to Neuropsychiatric PhenotypesJacobsen, Nick J. O. / Lyons, Ita / Hoogendoorn, Bastiaan / Burge, Susan / Kwok, Pui-Yan / O'Donovan, Michael C. / Craddock, Nick / Owen, Michael J. et al. | 1999
- 1637
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The Plasticity of Human Telomeres Demonstrated by a Hypervariable Telomere Repeat Array That Is Located on Some Copies of 16p and 16qColeman, Joanna / Baird, Duncan M. / Royle, Nicola J. et al. | 1999
- 1647
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Aberrant Interactions of Transcriptional Repressor Proteins with the Huntington's Disease Gene Product, HuntingtinBoutell, Jonathan M. / Thomas, Philip / Neal, James W. / Weston, Victoria J. / Duce, James / Harper, Peter S. / Lesley Jones, A. et al. | 1999
- 1657
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Nuclear Localization of the Spinocerebellar Ataxia Type 7 Protein, Ataxin-7Kaytor, Michael D. / Duvick, Lisa A. / Skinner, Pamela J. / Koob, Michael D. / Ranum, Laura P. W. / Orr, Harry T. et al. | 1999
- 1665
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Null Mutation of the Murine ATP7B (Wilson Disease) Gene Results in Intracellular Copper Accumulation and Late-Onset Hepatic Nodular TransformationBuiakova, Olesia I. / Xu, Jin / Lutsenko, Svetlana / Zeitlin, Scott / Das, Kamna / Das, Shonit / Ross, Barbara M. / Mekios, Constantinos / Scheinberg, I. Herbert / Gilliam, T. Conrad et al. | 1999
- 1673
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Isolation, characterization and mutation analysis of PEXI3-defective Chinese hamster ovary, cell mutantsToyama, R. / Mukai, S. / Itagaki, A. / Tamura, S. / Shimozawa, N. / Suzuki, Y. / Kondo, N. / Wanders, R. J. A. / Fujiki, Y. et al. | 1999
- 1673
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Isolation, Characterization and Mutation Analysis of PEX13-Defective Chinese Hamster Ovary Cell MutantsToyama, Ryusuke / Mukai, Satoru / Itagaki, Atsushi / Tamura, Shigehiko / Shimozawa, Nobuyuki / Suzuki, Yasuyuki / Kondo, Naomi / Wanders, Ronald J. A. / Fujiki, Yukio et al. | 1999
- 1683
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Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing HoloprosencephalyOdent, S. / Attié-Bitach, T. / Blayau, M. / Mathieu, M. / Augé, J. / Delezoïde, A.L. / Le Gall, J.Y. / Le Marec, B. / Munnich, A. / David, V. et al. | 1999
- 1691
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A Novel System for Assigning the Mode of Inheritance in Mitochondrial Disorders Using Cybrids and Rhodamine 6GWilliams, Andrew J. / Murrell, Melanie / Brammah, Susan / Minchenko, Jim / Christodoulou, John et al. | 1999
- 1699
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Mapping Recombination Hotspots in Human Phosphoglucomutase (PGM1)Ping Yip, Shea / Lovegrove, Jenny U. / Rana, Naheed A. / Hopkinson, David A. / Whitehouse, David B. et al. | 1999
- 1699
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Mapping recombination hotspots in human phosphoglucomutase (PGMI)Yip, S. P. / Lovegrove, J. U. / Rana, N. A. / Hopkinson, D. A. / Whitehouse, D. B. et al. | 1999
- 1707
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Combined Sib-TDT and TDT Provide Evidence for Linkage of the Interleukin-1 Gene Cluster to Erosive Rheumatoid ArthritisCox, Angela / Camp, Nicola J. / Cannings, Chris / di Giovine, Francesco S. / Dale, Mark / Worthington, Jane / John, Sally / Ollier, William E. R. / Silman, Alan J. / Duff, Gordon W. et al. | 1999
- 1715
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Sensitivity Issues in DNA Array-Based Expression Measurements and Performance of Nylon Microarrays for Small SamplesBertucci, François / Bernard, Karine / Loriod, Béatrice / Chang, Yi-Chung / Granjeaud, Samuel / Birnbaum, Daniel / Nguyen, Catherine / Peck, Konan / Jordan, Bertrand R. et al. | 1999
- 1723
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A Conserved Nuclear Element with a Role in Mammalian Gene RegulationDonnelly, Shaun R. / Hawkins, Tim E. / Moss, Stephen E. et al. | 1999
- 1729
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A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling PairsWilliams, N. M. / Rees, M. I. / Holmans, P. / Norton, N. / Cardno, A. G. / Jones, L. A. / Murphy, K. C. / Sanders, R. D. / McCarthy, G. / Gray, M. Y. et al. | 1999
- 1741
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The signal transducer and activator of transcription STAT5b gene is a new partner of retinoic acid receptor in acute promyelocytic-like leukaemiaArnould, C. / Philippe, C. / Bourdon, V. / Gregoire, M. J. / Berger, R. / Jonveaux, P. et al. | 1999
- 1741
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The Signal Transducer and Activator of Transcription STAT5b Gene Is a New Partner of Retinoic Acid Receptor {alpha} in Acute Promyelocytic-Like LeukaemiaArnould, Cécile / Philippe, Christophe / Bourdon, Violaine / Grégoire, Marie José / Berger, Roland / Jonveaux, Philippe et al. | 1999
- 1751
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Introduction of heteroplasmic mitochondrial DNA (mtDNA) from a patient with NARP into two human rho cell lines is associated either with selection and maintenance of NARP mutant mtDNA or failure to maintain mtDNAVergani, L. / Rossi, R. / Brierley, C. H. / Hanna, M. / Holt, I. J. et al. | 1999
- 1751
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Introduction of Heteroplasmic Mitochondrial DNA (MtDNA) from a Patient with NARP Into Two Human {rho}{degrees} cell Lines Is Associated Either With Selection and Maintenance of NARP Mutant MtDNA or Failure to Maintain MtDNAVergani, L. / Rossi, R. / Brierley, C. H. / Hanna, M. / Holt, I. J. et al. | 1999
- 1757
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Subcortical Band Heterotopia in Rare Affected Males Can be Caused by Missense Mutations in DCX (XLIS) or LIS1Pilz, Daniela T. / Kuc, Julie / Matsumoto, Naomichi / Bodurtha, Joann / Bernadi, Bruno / Tassinari, Carlo A. / Dobyns, William B. / Ledbetter, David H. et al. | 1999
- 1761
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Genetic Modification of Hearing in Tubby Mice: Evidence for the Existence of a Major Gene (moth1) Which Protects Tubby Mice from Hearing LossIkeda, Akihiro / Yin Zheng, Qing / Rosenstiel, Philip / Maddatu, Terry / Zuberi, Aamir R. / Roopenian, Derry C. / North, Michael A. / Naggert, Jürgen K. / Johnson, Kenneth R. / Nishina, Patsy M. et al. | 1999
- 1769
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Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly SyndromeKalff-Suske, Martha / Wild, Anja / Topp, Juliane / Wessling, Martina / Jacobsen, Eva-Maria / Bornholdt, Dorothea / Engel, Hartmut / Heuer, Heike / Aalfs, Cora M. / Ausems, Margreet G. E. M. et al. | 1999
- 1779
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French Machado-Joseph Disease Patients Do Not Exhibit Gametic Segregation Distortion: A Sperm Typing AnalysisGrewal, Raji P. / Cancel, Geraldine / Leeflang, Esther P. / Dürr, Alexandra / McPeek, Mary Sara / Draghinas, David / Yao, Xiang / Stevanin, Giovanni / Alnot, Marie-Odile / Brice, Alexis et al. | 1999
- 1785
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A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different NeurocristopathiesBondurand, Nadège / Kuhlbrodt, Kirsten / Pingault, Véronique / Enderich, Janna / Sajus, Marc / Tommerup, Niels / Warburg, Mette / Hennekam, Raoul C. M. / Read, Andrew P. / Wegner, Michael et al. | 1999
- 1791
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Altered Spacing of Promoter Elements Due to the Dodecamer Repeat Expansion Contributes to Reduced Expression of the Cystatin B Gene in EPM1Lalioti, Maria D. / Scott, Hamish S. / Antonarakis, Stylianos E. et al. | 1999
- 1799
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A Genome-Wide Scan Reveals a Maternal Susceptibility Locus for Pre-Eclampsia on Chromosome 2p13Arngrímsson, Reynir / Siguróaróóttir, Sigrún / Frigge, Michael L. / Bjarnaóóttir, Ragnheióur I. / Jónsson, Thorlákur / Stefánsson, Hreinn / Baldursdóttir, Ásdís / Einarsdóttir, Anna S. / Palsson, Birgir / Snorradôttir, Steinunn et al. | 1999
- 1807
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A Putative Drosophila Homolog of the Huntington's Disease GeneLi, Zhen / Karlovich, Chris A. / Fish, Matthew P. / Scott, Matthew P. / Myers, Richard M. et al. | 1999
- 1817
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Corrigenda| 1999