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<title><![CDATA[Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11]]></title>
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<title><![CDATA[Mutation of human short tandem repeats]]></title>
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<title><![CDATA[The DNA methyltransferases of mammals]]></title>
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<dc:title><![CDATA[Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene]]></dc:title>
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<title><![CDATA[The Rb/E2F pathway and cancer]]></title>
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<dc:title><![CDATA[The Rb/E2F pathway and cancer]]></dc:title>
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<title><![CDATA[Isolation of a candidate human telomerase catalytic subunit gene, which reveals complex splicing patterns in different cell types]]></title>
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<dc:title><![CDATA[Isolation of a candidate human telomerase catalytic subunit gene, which reveals complex splicing patterns in different cell types]]></dc:title>
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<title><![CDATA[Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy]]></title>
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<description><![CDATA[Henian Cao, Robert A. Hegele<br />Jan  1, 2000; 9:109-112<br />REPORTS]]></description>
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<dc:title><![CDATA[Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy]]></dc:title>
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<title><![CDATA[Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone]]></title>
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<dc:title><![CDATA[Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone]]></dc:title>
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<title><![CDATA[Heterogeneity in telomere length of human chromosomes]]></title>
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<dc:title><![CDATA[Heterogeneity in telomere length of human chromosomes]]></dc:title>
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<title><![CDATA[Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer]]></title>
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<dc:title><![CDATA[Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer]]></dc:title>
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<title><![CDATA[Decreased expression of striatal signaling genes in a mouse model of Huntington's disease]]></title>
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<dc:title><![CDATA[Decreased expression of striatal signaling genes in a mouse model of Huntington's disease]]></dc:title>
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<title><![CDATA[Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice]]></title>
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<dc:title><![CDATA[Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice]]></dc:title>
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<title><![CDATA[Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1]]></title>
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<description><![CDATA[Y Xue, X Gao, CE Lindsell, CR Norton, B Chang, C Hicks, M Gendron-Maguire, EB Rand, G Weinmaster, T Gridley<br />May  1, 1999; 8:723-730<br />ARTICLES]]></description>
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<dc:title><![CDATA[Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1]]></dc:title>
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<title><![CDATA[Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC]]></title>
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<dc:title><![CDATA[Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC]]></dc:title>
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<title><![CDATA[Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)]]></title>
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<description><![CDATA[Natascia Tiso, Dietrich A. Stephan, Andrea Nava, Alessia Bagattin, Joseph M. Devaney, Fabio Stanchi, Gaelle Larderet, Bhoomi Brahmbhatt, Kevin Brown, Barbara Bauce, Michela Muriago, Cristina Basso, Gaetano Thiene, Gian Antonio Danieli, Alessandra Rampazzo<br />Feb  1, 2001; 10:189-194<br />REPORTS]]></description>
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<dc:date>2001-02-01</dc:date>
<dc:identifier>10.1093/hmg/10.3.189</dc:identifier>
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<title><![CDATA[The survival motor neuron protein in spinal muscular atrophy]]></title>
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<title><![CDATA[Prediction of deleterious human alleles]]></title>
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<title><![CDATA[CREB-binding protein sequestration by expanded polyglutamine]]></title>
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<title><![CDATA[HIP-I: a huntingtin interacting protein isolated by the yeast two- hybrid system]]></title>
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<title><![CDATA[Mutations in the {{gamma}}2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis]]></title>
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<dc:title><![CDATA[Mutations in the {{gamma}}2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
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<title><![CDATA[A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease]]></title>
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<title><![CDATA[The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death]]></title>
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<dc:title><![CDATA[The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death]]></dc:title>
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<title><![CDATA[Analysis of myocilin mutations in 1703 glaucoma patients from five different populations]]></title>
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<dc:title><![CDATA[Analysis of myocilin mutations in 1703 glaucoma patients from five different populations]]></dc:title>
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<title><![CDATA[Methylation profiling of CpG islands in human breast cancer cells]]></title>
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<dc:title><![CDATA[The ABC of APC]]></dc:title>
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<title><![CDATA[Expansions of CAG repeat tracts are frequent in a yeast mutant defective in Okazaki fragment maturation]]></title>
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<dc:title><![CDATA[Expansions of CAG repeat tracts are frequent in a yeast mutant defective in Okazaki fragment maturation]]></dc:title>
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<title><![CDATA[SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein]]></title>
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<dc:title><![CDATA[SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein]]></dc:title>
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<title><![CDATA[Evidence that fragile X mental retardation protein is a negative regulator of translation]]></title>
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<description><![CDATA[Bernhard Laggerbauer, Dirk Ostareck, Eva-Maria Keidel, Antje Ostareck-Lederer, Utz Fischer<br />Feb  1, 2001; 10:329-338<br />ARTICLES]]></description>
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<dc:title><![CDATA[Evidence that fragile X mental retardation protein is a negative regulator of translation]]></dc:title>
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<title><![CDATA[Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polyglutamine aggregation in vitro]]></title>
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<description><![CDATA[Y Chai, SL Koppenhafer, SJ Shoesmith, MK Perez, HL Paulson<br />Apr  1, 1999; 8:673-682<br />ARTICLES]]></description>
<dc:creator>Y Chai, SL Koppenhafer, SJ Shoesmith, MK Perez, HL Paulson</dc:creator>
<dc:date>1999-04-01</dc:date>
<dc:identifier>10.1093/hmg/8.4.673</dc:identifier>
<dc:title><![CDATA[Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polyglutamine aggregation in vitro]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
</item>

<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/9/9/1415?rss=1&amp;ssource=mfc">
<title><![CDATA[Disruption of two novel genes by a translocation co-segregating with schizophrenia]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/9/9/1415?rss=1&amp;ssource=mfc</link>
<description><![CDATA[J. Kirsty Millar, Julie C. Wilson-Annan, Susan Anderson, Sheila Christie, Martin S. Taylor, Colin A. M. Semple, Rebecca S. Devon, David M. St Clair, Walter J. Muir, Douglas H. R. Blackwood, David J. Porteous<br />May 22, 2000; 9:1415-1423<br />REPORTS]]></description>
<dc:creator>J. Kirsty Millar, Julie C. Wilson-Annan, Susan Anderson, Sheila Christie, Martin S. Taylor, Colin A. M. Semple, Rebecca S. Devon, David M. St Clair, Walter J. Muir, Douglas H. R. Blackwood, David J. Porteous</dc:creator>
<dc:date>2000-05-22</dc:date>
<dc:identifier>10.1093/hmg/9.9.1415</dc:identifier>
<dc:title><![CDATA[Disruption of two novel genes by a translocation co-segregating with schizophrenia]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
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<title><![CDATA[The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn-/- mice and results in a mouse with spinal muscular atrophy]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/9/3/333?rss=1&amp;ssource=mfc</link>
<description><![CDATA[Umrao R. Monani, Michael Sendtner, Daniel D. Coovert, D. William Parsons, Catia Andreassi, Thanh T. Le, Sibylle Jablonka, Berthold Schrank, Wilfred Rossol, Thomas W. Prior, Glenn E. Morris, Arthur H.M. Burghes<br />Feb 12, 2000; 9:333-339<br />ARTICLES]]></description>
<dc:creator>Umrao R. Monani, Michael Sendtner, Daniel D. Coovert, D. William Parsons, Catia Andreassi, Thanh T. Le, Sibylle Jablonka, Berthold Schrank, Wilfred Rossol, Thomas W. Prior, Glenn E. Morris, Arthur H.M. Burghes</dc:creator>
<dc:date>2000-02-12</dc:date>
<dc:identifier>10.1093/hmg/9.3.333</dc:identifier>
<dc:title><![CDATA[The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn-/- mice and results in a mouse with spinal muscular atrophy]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
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<title><![CDATA[The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/5/7/1075?rss=1&amp;ssource=mfc</link>
<description><![CDATA[L Nistico, R Buzzetti, LE Pritchard, B Van der Auwera, C Giovannini, E Bosi, MT Larrad, MS Rios, CC Chow, CS Cockram, K Jacobs, C Mijovic, SC Bain, AH Barnett, CL Vandewalle, F Schuit, FK Gorus, R Tosi, P Pozzilli, JA Todd<br />Jul  1, 1996; 5:1075-1080<br />ARTICLES]]></description>
<dc:creator>L Nistico, R Buzzetti, LE Pritchard, B Van der Auwera, C Giovannini, E Bosi, MT Larrad, MS Rios, CC Chow, CS Cockram, K Jacobs, C Mijovic, SC Bain, AH Barnett, CL Vandewalle, F Schuit, FK Gorus, R Tosi, P Pozzilli, JA Todd</dc:creator>
<dc:date>1996-07-01</dc:date>
<dc:identifier>10.1093/hmg/5.7.1075</dc:identifier>
<dc:title><![CDATA[The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
</item>

<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/8/2/323?rss=1&amp;ssource=mfc">
<title><![CDATA[The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky- Pudlak syndrome and night blindness]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/8/2/323?rss=1&amp;ssource=mfc</link>
<description><![CDATA[L Feng, AB Seymour, S Jiang, A To, AA Peden, EK Novak, L Zhen, ME Rusiniak, EM Eicher, MS Robinson, MB Gorin, RT Swank<br />Feb  1, 1999; 8:323-330<br />ARTICLES]]></description>
<dc:creator>L Feng, AB Seymour, S Jiang, A To, AA Peden, EK Novak, L Zhen, ME Rusiniak, EM Eicher, MS Robinson, MB Gorin, RT Swank</dc:creator>
<dc:date>1999-02-01</dc:date>
<dc:identifier>10.1093/hmg/8.2.323</dc:identifier>
<dc:title><![CDATA[The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky- Pudlak syndrome and night blindness]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
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<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/7/9/1463?rss=1&amp;ssource=mfc">
<title><![CDATA[Huntingtin interacts with a family of WW domain proteins]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/7/9/1463?rss=1&amp;ssource=mfc</link>
<description><![CDATA[PW Faber, GT Barnes, J Srinidhi, J Chen, JF Gusella, ME MacDonald<br />Sep  1, 1998; 7:1463-1474<br />ARTICLES]]></description>
<dc:creator>PW Faber, GT Barnes, J Srinidhi, J Chen, JF Gusella, ME MacDonald</dc:creator>
<dc:date>1998-09-01</dc:date>
<dc:identifier>10.1093/hmg/7.9.1463</dc:identifier>
<dc:title><![CDATA[Huntingtin interacts with a family of WW domain proteins]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
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<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/6/1/105?rss=1&amp;ssource=mfc">
<title><![CDATA[Cancer risk associated with germline DNA mismatch repair gene mutations]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/6/1/105?rss=1&amp;ssource=mfc</link>
<description><![CDATA[MG Dunlop, SM Farrington, AD Carothers, AH Wyllie, L Sharp, J Burn, B Liu, KW Kinzler, B Vogelstein<br />Jan  1, 1997; 6:105-110<br />ARTICLES]]></description>
<dc:creator>MG Dunlop, SM Farrington, AD Carothers, AH Wyllie, L Sharp, J Burn, B Liu, KW Kinzler, B Vogelstein</dc:creator>
<dc:date>1997-01-01</dc:date>
<dc:identifier>10.1093/hmg/6.1.105</dc:identifier>
<dc:title><![CDATA[Cancer risk associated with germline DNA mismatch repair gene mutations]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
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<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/4/4/523?rss=1&amp;ssource=mfc">
<title><![CDATA[Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/4/4/523?rss=1&amp;ssource=mfc</link>
<description><![CDATA[Parsa Kazemi-Esfarjani, Mark A. Trifiro, Leonard Pinsky<br />Apr  1, 1995; 4:523-527<br />ARTICLES]]></description>
<dc:creator>Parsa Kazemi-Esfarjani, Mark A. Trifiro, Leonard Pinsky</dc:creator>
<dc:date>1995-04-01</dc:date>
<dc:identifier>10.1093/hmg/4.4.523</dc:identifier>
<dc:title><![CDATA[Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
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<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/10/14/1511?rss=1&amp;ssource=mfc">
<title><![CDATA[Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/10/14/1511?rss=1&amp;ssource=mfc</link>
<description><![CDATA[Christopher J. Cummings, Yaling Sun, Puneet Opal, Barbara Antalffy, Ruben Mestril, Harry T. Orr, Wolfgang H. Dillmann, Huda Y. Zoghbi<br />Jul  1, 2001; 10:1511-1518<br />REPORTS]]></description>
<dc:creator>Christopher J. Cummings, Yaling Sun, Puneet Opal, Barbara Antalffy, Ruben Mestril, Harry T. Orr, Wolfgang H. Dillmann, Huda Y. Zoghbi</dc:creator>
<dc:date>2001-07-01</dc:date>
<dc:identifier>10.1093/hmg/10.14.1511</dc:identifier>
<dc:title><![CDATA[Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
</item>

<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/10/10/1029?rss=1&amp;ssource=mfc">
<title><![CDATA[Contrasting effects on HIF-1{{alpha}} regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/10/10/1029?rss=1&amp;ssource=mfc</link>
<description><![CDATA[Steven C. Clifford, Matthew E. Cockman, Alan C. Smallwood, David R. Mole, Emma R. Woodward, Patrick H. Maxwell, Peter J. Ratcliffe, Eamonn R. Maher<br />May  1, 2001; 10:1029-1038<br />REPORTS]]></description>
<dc:creator>Steven C. Clifford, Matthew E. Cockman, Alan C. Smallwood, David R. Mole, Emma R. Woodward, Patrick H. Maxwell, Peter J. Ratcliffe, Eamonn R. Maher</dc:creator>
<dc:date>2001-05-01</dc:date>
<dc:identifier>10.1093/hmg/10.10.1029</dc:identifier>
<dc:title><![CDATA[Contrasting effects on HIF-1{{alpha}} regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
</item>

<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/9/4/645?rss=1&amp;ssource=mfc">
<title><![CDATA[Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/9/4/645?rss=1&amp;ssource=mfc</link>
<description><![CDATA[Patricia M. D''Cruz, Douglas Yasumura, Jessica Weir, Michael T. Matthes, Hadi Abderrahim, Matthew M. LaVail, Douglas Vollrath<br />Mar  1, 2000; 9:645-651<br />ARTICLES]]></description>
<dc:creator>Patricia M. D''Cruz, Douglas Yasumura, Jessica Weir, Michael T. Matthes, Hadi Abderrahim, Matthew M. LaVail, Douglas Vollrath</dc:creator>
<dc:date>2000-03-01</dc:date>
<dc:identifier>10.1093/hmg/9.4.645</dc:identifier>
<dc:title><![CDATA[Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
</item>

<item rdf:about="http://hmg.oupjournals.org/cgi/content/short/6/7/1177?rss=1&amp;ssource=mfc">
<title><![CDATA[Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1]]></title>
<link>http://hmg.oupjournals.org/cgi/content/short/6/7/1177?rss=1&amp;ssource=mfc</link>
<description><![CDATA[I Lemmens, WJ Van de Ven, K Kas, CX Zhang, S Giraud, V Wautot, N Buisson, K De Witte, J Salandre, G Lenoir, M Pugeat, A Calender, F Parente, D Quincey, P Gaudray, MJ De Wit, CJ Lips, JW Hoppener, S Khodaei, AL Grant, G Weber, S Kytola, BT Teh, F Farnebo, RV Thakker<br />Jul  1, 1997; 6:1177-1183<br />ARTICLES]]></description>
<dc:creator>I Lemmens, WJ Van de Ven, K Kas, CX Zhang, S Giraud, V Wautot, N Buisson, K De Witte, J Salandre, G Lenoir, M Pugeat, A Calender, F Parente, D Quincey, P Gaudray, MJ De Wit, CJ Lips, JW Hoppener, S Khodaei, AL Grant, G Weber, S Kytola, BT Teh, F Farnebo, RV Thakker</dc:creator>
<dc:date>1997-07-01</dc:date>
<dc:identifier>10.1093/hmg/6.7.1177</dc:identifier>
<dc:title><![CDATA[Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
</item>

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