Report of the Third International Workshop on human chromosome 18 mapping 1995.

titles of thethird international workshop on human chromosome 18 mapping 1995 Author listed in bold type presented the abstract at the workshop.The com plete abstract can be found in the GDB (GDB ID Number). D. Adamson, H. Albertsen, L. Ballard, P. Bradley, M. Carlson, P.Cartwright, T. Eisner, D. Fuhrman, S. Gerken, L. Harris, P.R Holik,A. Kimball, J. Knell, E. Lawrence, J. Lu, A. Marks, N, Matsunami,R. Melis, B. Milner, M. Moore, L. Nelson, S. Odelberg, G. Peters,R. Plaetke, R. Riley, M. Robertson, R. Sargent, G. Staker, A.Tingey, K. Ward, X. Zhao and R. WhiteE.D. Carstea,1 K.G. Coleman,1 D. Zhang,1 M.T. Vanier,2 M.H.Polymeropoulos^ and P.G. Pentchev1National Institute of Neurological Disorders and Stroke, NationalInstitutes of Health, Bethesda MD, USA, ^INSERM U189, Lyon-SSchool of Medicine, Lyon, France, ^National Center for HumanGenome Research, Bethesda MD, USADepartment of Human Genetics, University of Utah Health SciencesLocalizing the human Nlemann-PIck disease type c gene toCenter, Salt Lake City UT, USAA PCR-based genetic linkage map of human chromosome 18(G00-592-404) L. Ala-Kokko,1 J. Vuoristo,1 J. Overhauser,1 T. Ferraro,2 W.Berrettini,2 and D.J. Prockop1Department of Biochemistry and Molecular Biology, and^Department of Psychiatry and Human Behaviour, Thomas JeffersonUniversity, Philadelphia PA, USAThe gene for the g-protein G-olf a tissue specific expressionas mRNA with variable length 3’-non-translated regions (GOO-592-397) J. Arnemann,1 D. Simrak1, C.M.E. Cowley2 and R.S. Buxton2lInstitut for Humangenetik, Universitätsklinik, Frankfurt/M.Germany. Division of Eukaryotic Molecular Genetics, NationalInstitute for Medical Research, The Ridgeway, Mill Hill, London,United KingdomA YAC contig for the desmosomal cadherin locus at 18q12.1(GOO-592-403) W.H. Berrettini,1 T.N. Ferraro1, J. Vuoristo,2 L. Ala-Kokko,2 R.Goldin,3 S.D.-Detera-Wadleigh,3 J.l. Nürnberger, Jr. 3 and E.S.Gershon3l2Department of Psychiatry, ^Biochemistry and Molecular Biology,Thomas Jefferson University, Philadelphia PA, ^National Institute ofMental Health, National Institute of Health, Bethesda MD, USAA linkage study of bipolar illness (GOO-592-385) L. Boghoslan-Sell and J. OverhauserDepartment of Biochemistry and Molecular Biology, ThomasJefferson University, Philadelphia PA, USACharacterization of a (7; 18) chromosome translocationbreakpoint that segregates in a family with features ofTourette's syndrome (G0Q-592-406) K.H. Buetow,1 V. Sheffield,2 G. Duyk,3 J. Weber,4 and J. Murray2^Fox Chase Cancer Center, Philadelphia PA; ^University of Iowa,Iowa City IA; ^Harvard University, Cambridge MA; ^MarshfieldMedical Research Foundation, Marshfield WI, USAA genetic map of human chromosome 18 (G00-592-4Q9)18q11 A.J. CuticchlaDivision of Biomedicai Information Sciences, Johns HopkinsUniversity, Baltimore MD, USA and thè Genome Data BaseThe role of thè Genome Data Base at thè chromosome 18workshop (G00-592-393) B. de Leeuw, M. Balemans, D. Olde Weghuis and A. Geurts vanKesselDepartment of Human Genetics, University Hospital, Nijmegen, TheNetherlandsIdentification of two alternative fusion genes, SYT-SSX1 andSYT-SSX2, in t(X;18)(p11.2;q11.2)-positive synovial sarcomas(GOO-592-386) S.D. Detera-Wadleigh,1 T. Yoshikawa,1 W.H. Berrettini,2 L.R.Goldin,1 and E.S. Gershon1*National Institute of Mental Health, National Institutes of Health,•^Thomas Jefferson University, USACandidate genes for bipolar illness on chromosome 18 (G00-592-400) N. Freimer,1 S. Baharloo,1 V. Carlton,1 L. Bull,1 N. Huynh,1 B.Scharschmidt,1 N. Lomri,1 A. Knisely,2 R. Houwen31University of California, San Francisco, San Francisco CA;2Childrens Hospital and University of Pittsburgh, Pittsburgh PA,USA; 3Wilhelmina Childrens Hospital, Utrecht, T he NetherlandsFine mapping of a locus for familial cholestasis in 18q21 (GOO592-405) A.J. Griffith, D.C. Kohrman, D.L. Burgess, and M.H. MeislerDepartment of Human Genetics, University of Michigan, Ann A it) orMI, USAComparative mapping of a disease gene linkage marker onhuman and mouse chromosome 18 (G00-592-396) R.H.J. Houwen,1 J.K. Ploos van Amster,2 R. Berger,1 and N.Freimer312Wilhelmina Childrens Hospital, ^Clinical Genetics Center Utrecht,The Netherlands, Neurogenetics Laboratory, University ofCalifornia, San Francisco CA, USAThe BRIC gene is localized between the markers D18s69 andD18s60 (G00-592-390) 118Cytogenet Cell Genet, Vol. 71,1995 A.E. Hughe«,1 A.M. Shearman,1 K.J. May,1 D.J. Housman,2 andN.C. Nevin1department of Medical Genetics, The Queen’s University of Belfast,UK; ^Center for Cancer Research, MIT, Cambridge MA, USAPhysical mapping of the familial expansile osteolysis region inchromosome 18q21.3 (G00-592-401)P. O’Connell,1'2 2. Brkanac,1 and R.J. Leach11Department o f Cellular and Structural Biology, department ofPathology, University o f Texas Health Science Center, San AntonioTX, USASTS content-based YAC map of distal long arm of humanchromosome 18 (GOO-592-398) A. Kimura,1 H. Harada, and J. Overhauser2department of Tissue Physiology, Division o f Adult Diseases,Medical Research Institute, Tokyo Medical and Dental University,Tokyo, Japan and departm ent of Biochemistry and MolecularBiology, Thomas Jefferson University, Philadelphia PA, USA.Isolation, characterization and mapping of a human RIC genefamily on the short arm of chromosome 18 (G00-592-411) 1,1 S.-J. Yoon,1 J. LeBlanc-K.S. Krauter,1 K. MontgomeryStraceski,1 B. Renault, ‘ L. Cupelli,1 I. Marondel,1 V. Herdman,1 A.Banks,2 J. Lieman,2 J. Menninger,2,P. Bray-Ward,2 P. Nadkarni,2J. Weissenbach,3 1. Chumakov,4 D. Cohen,4 P. Miller,2 D. Ward,2and R. Kuckerlapati11Albert Einstein College of Medicine, Bronx NY; Yale UniversitySchool of Medicine, New Haven CT, LISA; denethon, Evry Cedex,France; 4CEPH, Paris, France.An Integrated physical map of human chromosome 12 (GOO-592-394)J. Overhauser, K. Rojas, G. Strathdae, and G. SilvermanDepartment of Biochemistry and Molecular Biology, ThomasJefferson University, Philadelphia PA, USASomatic cell hybrid mapping panel for chromosome 18 (GOO592-407) M.C. Petrosso,1 P. Gobbi,2 P. Conigli,3 F. Salvi,2 P. Vezzoni,1 andA. Ferllni3'41 CNR, Milano, -^Servizio di Neurologia, Ospedale Bellaria,d iv is io n e di Neurologia, Arcispedale S. Anna, Ferrara, Italy,UKTransthyretin (TTR) gene: identification of nevigenotype-phenotype correlation (G00-592-402) C. Schick, S.S. Schneider, S.D. Treterand G.A. SilvermanDepartment o f Pediatrics, Harvard Medical School, Boston MA, USAA family of human serine proteinase Inhibitors map to 18q21.3(GOO -592-388) R.J. Leach and J.D. CodyThe University of Texas Health Science Center, San Antonio TX,USARadiation-reduced hybrid panel for human chromosome 18(G00-592-399) T. Mansfield,1 F. Leach,2 N. Lisitsyn,3 M. Wîgler,3 B. Vogelstein,3and E. Fearon1lG. Sirugo,1 T. Haaf,1 J. Parnas,2 S. Matthysse,3 D. Levy,3 P.Holzman3 and K.K. Kidd1*Yale University, Department of Genetics, School of Medicine, NewHaven CT, USA; Department of Preventive Medicine,Kommunehospitalet, Copenhagen Denmark; Department ofPsychiatry, Hvidovre Hospital, Denmark and 3McLean Hospital,Belmont MA, and Harvard Medical School, Boston MA, USA.Repeat expansion detection (RED) of a (CTG)n dynamicmutation In a Danish schizophrenia kindred, mapped toYale University, New Haven CT, 2Johns Hopkins University,Baltimore MD, *Cold Spring Harbor Laboratory, Cold Spring Harborchromosome 18q21 by in situ hybridization. (G00-592-392)NY, USALoss of heterozygosity on chromosome 18q in a colorectalcancer (G00-592-391 ) M. Muenke1 and J. Overhauser2The Children’s Hospital of Philadelphia and Department ofPediatrics, Division of Human Genetics and Molecular Biology,University of Pennsylvania School of Medicine, Philadelphia PA;Department of Biochemistry and Molecular Biology, ThomasJefferson University, Philadelphia PA, USADefinition of the holoprosencephaly minimal critical region(MCR) on chromosome 18p (G00-592-410)O.C. Stine,1 J. Xu,1 R. Koskela,2 F.J. McMahon,1 C.D. Clark,3 C.Friddle 3 M. Geshwant,3 T, Breschel,1 S.G. Simpson,1 D.Botstein,3 T.G. Marr,2 M.G. Mclnnis,1 D.A. Meyers,4 and J.R.DePaulo1department of Psychiatry, John Hopkins University School ofMedicine, Baltimore MD; department of Computational Biology,Cold Spring Harbor Laboratory, Cold Spring Harbor, NY;department of Genetics, Stanford University, Stanford, CA;department o f Medicine, John Hopkins University School of Evidence for linkage of bipolar disorder to chromosome 18with a parent-of-orlgln effect (G00-592-389) H. Nakashima, M. Sakai, R. Inaba, and T. ImamuraDepartment of Human Genetics, National Institute of Genetics,Mishima, JapanConstruction of human chromosome 18 cosmid library andmapping of 60 new probes using fluorescence in situhybridization (G00-592-387)G. Strathdee,1 E.H. Zackai,2 R. Shapiro,3 J. Kamholz,4 J.Overhauser1‘Department of Biochemistry and Molecular Biology, ThomasJefferson University, Philadelphia PA; department of Genetics,^Psychiatry, and ‘̂ Neurology,Medicine, Philadelphia PA, USAMolecular cytogenetic analysis of 18q* syndrome (G0Q-592408) Cytogenet Cell Genet, Vol. 71,1995•1119