Third International Chromosome 1 Maping Workshop, Duke University, Durham, NC, USA, 25-27 April 1997: Report of the third international workshop on human chromosome 1 mapping 1997

Cytogenetics and Cell Genetics

Volumn 78, Issue 3-4, 1997, Pages 154-179

  Vance, Jeffery M ^a,i   Matise, T C ^b   Wooster, R ^c   Schutte, B C ^d   Bruns, G A P ^e   Van Roy, N ^f   Brodeur, G M ^g   Tao, Y X ^a   Gregory, S ^c   Weith, A ^h   Vaudin, M ^c   White, P ^g  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b ROCKEFELLER UNIVERSITY   (United States)

^c WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^d UNIVERSITY OF IOWA   (United States)

^e BOSTON CHILDREN S HOSPITAL   (United States)

^f GHENT UNIVERSITY HOSPITAL   (Belgium)

^g CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^h RESEARCH INSTITUTE OF MOLECULAR PATHOLOGY   (Austria)

ⁱ DUKE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CANCER GENETICS; CHROMOSOME 1P; CHROMOSOME 1Q; CHROMOSOME ABERRATION; CHROMOSOME MAP; CONFERENCE PAPER; GENE LOCUS; GENETIC DISORDER; GENOME; PRIORITY JOURNAL; SEQUENCE ANALYSIS; CHROMOSOME 1; CHROMOSOME DISORDER; COMPUTER NETWORK; DNA SEQUENCE; FACTUAL DATABASE; HUMAN; RADIATION CHIMERA;

CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; COMPUTER COMMUNICATION NETWORKS; DATABASES, FACTUAL; HUMANS; RADIATION CHIMERA; SEQUENCE ANALYSIS, DNA;

EID: 0031304821     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (180)

1. Abraham JM, Wang S, Suzuki H, Jiang HY, Rosenblumvos LS, Yin J, Meltzer SJ: Esophagin cDNA cloning and characterization - a tissue-specific member of the small proline-rich protein family that is not expressed in esophageal tumors. Cell Growth Diff 7:855-860 (1996).
2. Aho H, Schwemmer M, Tessmann D, Murphy D, Mattei G, Engel W, Adham I: Isolation, expression, and chromosomal localization of the human mitochondrial capsule selenoprotein gene (MCSP). Genomics 32:184-190 (1996).
3. Akarsu AN, Turacli ME, Aktan SG, Barsoum Homsy M, Chevrette L, Sayli BS, Sarfarazi M: A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region. Hum Mol Genet 5:1199-1203 (1996).
4. Albertin G, Rossi GP, Majone F, Tiso N, Mattara A, Danieli GA, Pessina AC, Palu G: Fine mapping of the human endothelin-converting enzyme gene by fluorescent in situ hybridization and radiation hybrids. Biochem biophys Res Commun 221:682-687 (1996).
5. Albig W, Ebentheuer J, Klobeck G, Kunz J, Doenecke D: A solitary human H3 histone gene on chromosome 1. Hum Genet 97:486-491 (1996).
6. Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, Gerrard B, Baird L, Stauffer D, Peiffer A, Rattner A, Smallwood P, Li Y, Anderson KL, Lewis RA, Nathans J, Leppert M, Dean M, Lupski JR: A photoreceptor cell-specific ATP binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nature Genet 15:236-246 (1997).
7. Antonacci R, Marzella R, Finelli P, Lonoce A, Forabosco A, Archidiacono N, Rocchi M: A panel of subchromosomal painting libraries representing over 300 regions of the human genome. Cytogenet Cell Genet 68:25-32 (1995).
8. Aplan PD, Raimondi SC, Kirsch IR: Disruption of the SCL gene by a t(1 ;3) translocation in a patient with T-cell acute lymphoblastic leukemia. J exp Med 176:1301-1310 (1992).
9. Arlt MF, Herzog TJ, Mutch DG, Gersell DJ, Liu H, Goodfellow PJ: Frequent deletion of chromosome 1p sequences in an aggressive histologic subtype of endometrial cancer. Hum Mol Genet 5:1017-1021 (1996).
10. Ariyama T, Inazawa J, Ezaki T, Nakamura Y, Horii A, Abe T: High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: the precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs. Genomics 25:114-23 (1995).
11. Bader S, Fasching C, Brodeur GM, Stanbridge E: Dissociation of suppression of tumorigenicity and differentiation in vitro effected by transfer of single human chromosomes into human neuroblastoma cells. Cell Growth Diff 2:245-255 (1991).
12. Barnas CM, Onyango P, Ellmeier W, Lengauer C, Kleiner E, Henn T, Brunner C, Stapleton P, Weith A: Determination and regional assignment of grouped sets of microclones in chromosome 1 pter→p35. Genomics 29:607-615 (1995).
13. Barr FG, Nauta LE, Davis RJ, Schafer BW, Nycum LM, Biegel JA: In vivo amplification of the PAX3-FKHR and PAX7-FKHR fusion genes in alveolar rhabdomyosarcoma. Hum Mol Genet 5:15-21 (1996).
14. Barrat FJ, Auloge L, Pastural E, Lagelouse RD, Vilmer E, Cant AJ, Weissenbach J, Le Paslier D, Fischer A, de Saint Basile G: Genetic and physical mapping of the Chediak-Higashi syndrome on chromosome 1q42→q43. Am J hum Genet 59:625-632 (1996).
15. Barron-Casella EA, Torres MA, Scherer SW, Heng HH, Tsui LC, Casella JF: Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families. J biol Chem 270:21472-21479 (1995).
16. Bello MJ, Leone PE, Nebreda P, de Campos JM, Kusak ME, Vaquero J, Sarasa JL, Garcia-Miguel P, Queizan A, Hernandez-Moneo JL, Pestana A, Rey JA: Allelic status of chromosome 1 in neoplasms of the nervous system. Cancer Genet Cytogenet 83:160-164 (1995a).
17. Bello MJ, Leone PE, Vaquero J, de Campos JM, Kusak ME, Sarasa JL, Pestana A, Rey JA: Allelic loss at 1p and 19q frequently occur in association and may represent early oncogenic events in oligodendroglial tumors. Intl J Cancer 64:207-210 (1995b).
18. Beltinger CP, White PS, Maris JM, Sulman EP, Jensen SJ, Paslier LD, Stallard BJ, Goeddel DV, de Sauvage FJ, Brodeur GM: Physical mapping and genomic structure of the human TNFR2 gene. Genomics 35:94-100 (1996).
19. Byers TJ, Beggs AH, McNally EM, Kunkel LM: Novel actin crosslinker superfamily member identified by a two step degenerate PCR procedure. FEBS Lett 368:500-504 (1995).
20. Bieche I, Champeme MH, Lidereau R: A tumor suppressor gene on chromosome 1 p32 → pter controls the amplification of MYC family genes in breast cancer. Cancer Res 54:4274-4276 (1994).
21. Bjorkqvist AM, Tammilehto L, Anttila S, Mattson K, Knuutila S: Recurrent DNA copy number changes in 1q, 4q, 6q, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma. Brit J Cancer 75:523-527 (1997).
22. Bray-Ward P, Menninger J, Lieman J, Desai T, Mokady N, Banks A, Ward DC: Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones. Genomics 32:1-14 (1996).
23. Burnett RC, Thirman MJ, Rowley JD, Diaz MO: Molecular analysis of the T-cell acute lymphoblastic leukemia-associated t(1 ;7)(p34;q34) that fuses LCK and TCRB. Blood 84:1232-1236 (1994).
24. Buyse IM, Takahashi EI, Huang S: Physical mapping of the retinoblastoma interacting zinc finger gene RIZ to D1S228 on chromosome 1p36. Genomics 34:119-121 (1996).
25. Byrne PC, Shipley JM, Chave KJ, Sanders PG, Snell K: Characterisation of human serine hydroxymethlytrasferase pseudogene and its localisation of 1 p32.3→p33. Hum Genet 97:340-344 (1996).
26. Carnemolla B, Leprini A, Borsi L, Querze G, Urbini S, Zardi L, Sandrin MS, Henning MM, Lo MF, Baker E, Sutherland GR, McKenzie IF: Human tenascin-R. Complete primary structure, pre-mRNA alternative splicing and gene localization on chromosome 1q23→q24.J biol Chem 271:8157-8160 (1996).
27. Casciano I, Marchi JV, Muresu R, Volpi EV, Rozzo C, Opdenakker G, Romani M: Molecular and genetic studies on the region of translocation and duplication in the neuroblastoma cell line NGP at the 1p36.13→p36.32 chromosomal site. Oncogene 12:2101-2108 (1996).
28. Cerretti DP, Lyman SD, Kozlosky CJ, Copeland NG, Gilbert DJ, Jenkins NA, Valentine V, Kirstein MN, Shapiro DN, Morris SW: The genes encoding the EPH-related receptor tyrosine kinase ligands LERK-1 (EPLG1, Ep11), LERK-3 (EPLG3, Ep13), and LERK-4 (EPLG4, Ep14) are clustered on human chromosome 1 and mouse chromosome 3. Genomics 33:277-282 (1996).
29. Chang ML. Eddy RL, Shows TB, Lau JT: Three genes that encode human beta-galactoside alpha 2,3-sialyltransferases. Structural analysis and chromosomal mapping studies. Glycobiology 5:319-325 (1995).
30. Chang PWG, Tsui SKW, Liew CC, Lee CY, Waye MMY, Fung KP: Isolation, characterization, and chromosomal mapping of a novel cDNA clone encoding human selenium binding protein. J Cell Biochem 64:217-224 (1997).
31. Chase PB, Yang JM, Thompson FH, Halonen M, Regan JW: Regional mapping of the human platelet-activating factor receptor gene (PTAFR) to 1p35→p34.3 by fluorescence in situ hybridization. Cytogenet Cell Genet 72:205-207 (1996).
32. Chen HL, Chen YC, Chen DS: Chromosome l p aberrations are frequent in human primary hepatocellular carcinoma. Cancer Genet Cytogenet 86:102-106 (1996).
33. Cheng NC, Chan AJK, Beitsma MM, Speleman F, Westerveld A, Verstegg R: A human modifer of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35→p36.1. Hum Molec Genet 5:309-3-7 (1996).
34. Chung WK, Power-Kehoe L, Chua M, Leibel RL: Mapping of the OB receptor to 1p in a region of nonconserved gene order from mouse and rat to human. Genome Res 6:431-438 (1996).
35. Clancy KP, Berger R, Cox M, Bleskan J, Walton KA, Hart I, Patterson D: Localization of the L-glutamine synthetase gene to chromosome 1q23. Genomics 38:418-420 (1996).
36. Clepet C, Dauwerse HJ, Desmaze C, van Ommen GJB, Weissenbach J, Morissette J: A 10-cM YAC contig spanning GLC1 A, the primary open-angle glaucoma locus at 1q23→q25. Eur J hum Genet 4:250-259 (1996).
37. Collins A, Frezal J, Teague J, Morton N: A metric map of humans, 23,500 loci in 850 bands. Proc natl Acad Sci, USA 93:14771-14775 (1996).
38. Cox DR, Burmeister M, Price ER, Kim S, Myers RM: Radiation hybrid mapping: A somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes Science 250:245-250 (1990).
39. Cryns VL, Yi SM, Tahara H, Gaz RD, Arnold A: Frequent loss of chromosome arm 1p DNA in parathyroid adenomas. Genes Chrom Cancer 13:9-17 (1995).
40. Dausset J, Cann H, Cohen D, Lathrop M, Lalouel J-M, White R: Centre d'Etude du Polymorphisme Humain (CEPH): Collaborative genetic mapping of the human genome. Genomics 6:575-577 (1990).
41. Davis RJ, D-Cruz CM, Lovell MA, Biegel JA, Barr FG: Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma. Cancer Res 54:2869-2872 (1994).
42. Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan, J Seboun E, et al.: A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154 (1996).
43. Dracopoli NC, Brouns GAP, Brodeur GM, Landes GM, Matise TC, Seldin M, Vance JM, Weith A: Report of the first international workshop on human chromosome 1 mapping 1994. Cytogenet Cell Genet 67:144-165 (1994).
44. Durbin R, Mieg JR: A C Elegans Database. Documentation, code, and data available from anonymous FTP servers at lirmm.lirmm. fr, cele.mrc1mb.cam.ac.uk and ncbi.nlm.nih.gov (1991).
45. Eiberg H, Lund AM, Warburg M, Rosenberg T: Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36. Hum Genet 96:3338 (1995).
46. Eki T, Okumura K, Amin A, Ishiai M, Abe M, Nogami M, Taguchi H, Hurwitz J, Murakami Y, Hanaoka F: Mapping of the human homologue (ORC1L) of the yeast origin recognition complex subunit 1 gene to chromosome band 1p32. Genomics 36:559-561 (1996).
47. Ezaki T, Yanagisawa A, Ohta K, Also S, Watanabe M, Hibi T, Kato Y, Nakajima T, Ariyama T, Inazawa J, Nakamura Y, Horii A: Deletion mapping on chromosome 1p in well-differentiated gastric cancer. Brit J Cancer 73:424-428 (1996).
48. Fagan KP, Oliveira L, Pittler SJ: Sequence of rho small GTP-binding protein cDNAs from human retina and identification of novel 5′ end cloning artifacts (letter). Exp Eye Res 59:235-237 (1994).
49. Fagerheim T. Nilssen O, Raeymaekers P, Brox V, Mourn T, Elverland HH, Teig E, Omland HH, Fostad GK, Tranebjaerg L: Identification of a new locus for autosomal dominant nonsyndromic hearing impairment (DFNA7) in a large Norwegian family. Hum Mol Genet 5:1187-1191 (1996).
50. Fink JM, Hirsch BA, Zheng C, Dietz G, Hatten ME, Ross ME: Astrotactin (ASTN), a gene for glialguided neuronal migration, maps to human chromosome 1q25.2.Genomics 40:202-205 (1997).
51. Fitzgerald TJ, Neale GAM, Raimondi S, Goorha RM: c-TAL, a helix-loop-helix protein, is juxtaposed to the T-cell receptor-B chain gene by a reciprocal chromosomal translocation: t(1p7)(q32;q35). Blood 78:2686-2695 (1991).
52. Fitzgibbon J, Katsanis N, Wells D, Delhanty J, Vallins W, Hunt DM: Human guanylate kinase (GUK1): cDNA sequence, expression and chromosomal localization. FEBS Letters 385:185-188 (1996).
53. Forabosco P, Collins A, Morton NE: Integration of gene maps: updating chromosome 1. Ann Hum Genet 59:291-305 (1995).
54. Frezal AJ, Teague J, Morton N: A metric map of humans, 23,500 loci in 850 bands. Proc natl Acad Sci, USA 93:14771-14775 (1996).
55. Fukai K, Oh J, Karim MA, Moore KJ, Kandil HH, Ito H, Burger J, Spritz RA. Homozygosity mapping of the gene for ChediakHigashi syndrome to chromosome 1 q42→q44 in a segment of conserved synteny that includes the mouse beige locus (bg). Am J human Genet 59:620-624 (1996).
56. Furukawa Y, Kawakami T, Sudo K, Inazawa J, Matsumine A, Akiyama T, Nakamura Y: Isolation and mapping of a human gene (RPD3L1) that is homologous to RPD3, a transcription factor in Saccharomyces cerevisiae. Cytogenet Cell Genet 73:130-133 (1996).
57. Futreal PA, Gumbs C, Berchuck A, Weissman RW: Frequent allelic deletion of chromosome 1p in primary ovarian cancer: Mapping of two tumor suppressor gene regions and preliminary analysis of candidate genes. Am J hum Genet 57:A#11 (1995).
58. Gebe JA, Kiener PA, Ring HJZ, Li X, Francke U, Aruffo A: Molecular cloning, mapping to human chromosome 1q21→q23, and cell binding characteristics of sp-alpha, a new member of the scavenger receptor cysteine-rich (Srcr) family of proteins. J biol Chem 272:6151-6158 (1997).
59. Gelb BD, Edelson JG, Desnick RJ: Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mapping. Nature Genet 10:235-237 (1995).
60. Gelb BD, Shi GP, Chapman HA, Desnick RJ: Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science 273:1236-1238 (1996).
61. Gelb BD, Zhang J, Cotter PD, Gershin IF, Desnick RJ: Physical mapping of the human connexin 40 (GJA5), flavin-containing monooxygenase 5, and natriuretic peptide receptor A genes on 1q21. Genomics 39:409-411 (1997).
62. Greco A, Villa R, Pierotti MA: Genomic organization of the human NTRK1 gene. Oncogene 13:2463-2466 (1996).
63. Grover J, Chen XN, Korenberg JR, Recklies AD, Roughley PJ: The gene organization, chromosome location, and expression of a 55-kDa matrix protein (PRELP) of human articular cartilage. Genomics 38:109-117 (1996).
64. Gyapay G, Schmitt K, Fizames C, Jones H, Vega-Czarny N, Spillett D, Muselet D, Prud'Homme JF, Dib C, Auffray C, Morissette J, Weissenbach J, Good-fellow PN: A radiation hybrid map of the human genome. Hum Mol Genet 5:339-346 (1996).
65. Hardas BD, Zhao X, Zhang J, Longqing X, Stoll S, Elder JT: Assignment of psoriasin to human chromosomal band 1q21 : coordinate overexpression of clustered genes in psoriasis. J Invest Dermatol 106:753-758 (1996).
66. Hashimoto N, Ichikawa D, Arakawa Y, Date K, Ueda S, Nakagawa Y, Horii A, Nakamura Y, Abe T, Inazawa J: Frequent deletions of material from chromosome arm 1p in oligodendroglial tumors revealed by double-target fluorescence in situ hybridization and microsatellite analysis. Genes Chrom Cancer 14:295-300 (1995).
67. Hellsten E, Vesa J, Heiskanen M, Makela TP, Jarvela I, Cowell JK, Mead S, Alitalo K, Palotie A, Peltonen L: Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus. Genomics 25:404-412 (1995).
68. Hirai M, Kusuda J, Hashimoto K: Assignment of human ADP ribosylation factor (ARF) genes ARF1 and ARF3 to chromosomes 1q42 and 12q13, respectively. Genomics 34:263-265 (1996).
69. Hoggard N, Hey Y, Brintnell B, James L, Jones D, Mitchell E, Weissenbach J, Varley JM: Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer. Genomics 30:233-243 (1995).
70. Horikawa I, Yamada H, Kugoh H, Yuasa Y, Suzuki M, Oshimura M: Subchromosomal mapping of a putative transformation suppressor gene on human chromosome 1. Jpn J Cancer Res 86:444-450 (1995).
71. Hu CA, Lin WW, Valle D: Cloning, characterization, and expression of cDNAs encoding human delta l-pyrroline-5-carboxylate dehydrogenase. J biol Chem 271:9795-9800 (1996).
72. Hudson TJ, Stein LD, Gerety S, Ma J, Castle A, Suva J, Slonim D, Baptista R, Kruglyak L, Xu S: An STS-based map of the human genome. Science 270:1945-1954 (1995).
73. Iaonnou PA, Amemiya CT, Games J, Kroisel PM, Shizuya H, Chen C, Batzer MA, de Jong PJ: A new bacteriophage P1-derived vector for the propagation of large human DNA fragments. Nature Genet 6:84-89 (1994).
74. Ionides ACW, Berry V, Mackay DS, Moore AT, Bhattacharya S, Shiels A: A locus for autosomal dominant posterior polar cataract on chromosome 1p. Hum Mol Genet 6:4751 (1997).
75. Jensen SJ, Sulman EP, Maris JM, Matise TC, Vojta PJ, Barren JC, Brodeur GM, White PS: An integrated transcript map of human chromosome lp35→ p36. Genomics 42:126-136 (1997).
76. Jung BP, Nguyen T, Kolakowski LF Jr, Lynch KR, Heng HH, George SR, O'Dowd BF: Discovery of a novel human G protein-coupled receptor gene (GPR25) located on chromosome 1. Biochem biophys Res Comm 230:69-72 (1997).
77. Karlsson C, Stenman G, Vojta PJ, Bongcam-Rudloff E, Barrett JC, Westermark B, Paulsson Y: Escape from senescence in hybrid cell clones involves deletions of two regions located on human chromosome 1q. Cancer Res 56:241-245 (1996).
78. Kirn U-J, Birren B, Mancino V, Slepak T, Boysen C, Kang H-L, Simon MI, Shizuya H: Construction and characterization of a human bacterial artificial chromosome library. Genomics 34:213-218 (1996).
79. Kingsmore SF, Souryal CA, Watson ML, Patel DD, Seldin MF: Physical and genetic linkage of the genes encoding LY-9 and CD48 on mouse and human chromosome 1. Immunogenet 42:59-62 (1995).
80. Koi M, Shimizu M, Morita H, Yamada H, Oshimura M: Construction of mouse A9 clones containing a single human chromosome tagged with neomycinresistance gene via microcell fusion. Jpn J Cancer Res 80:413-418 (1989).
81. Kozlov SV, Giger RJ, Hasler T, Korvatska E, Schorderet DF, Sonderegger P: The human TAXI gene encoding the axon-associated cell adhesion molecule TAG-1 /axonin-1 : genomic structure and basic promoter. Genomics 30:141-148 (1995).
82. Kraus JA, Albrecht S, Wiestier OD, von Schweinitz D, Pietsch T: Loss of heterozygosity on chromosome 1 in human hepatoblastoma. Int J Cancer 67:467-471 (1996a).
83. Kraus JA, Koch A, Albrecht S, Von Deimling A, Wiestier OD: Loss of heterozygosity at locus F1 3B on chromosome 1q in human medulloblastoma. IntJ Cancer 67:11-15 (1996b).
84. Kugoh H, Nakagawa Y, Mitsuya K, Mita T, Suzuki M, Suzuki N, Uejima H, Yuasa Y, Oshimura M: Isolation and mapping of 186 new DNA markers on human chromosome 1. Genomics 27:207-210 (1995).
85. Kuroki T, Fujiwara Y, Tsuchiya E, Nakamori S, Imaoka S, Kanematsu T, Nakamura Y: Accumulation of genetic changes during development and progression of hepatocelllar carcinoma: Loss of heterozygosity on chromosome 1 occurs at an early stage of hepatocarcinogenesis. Genes Chrom Cancer 13:163-167 (1995).
86. Kusuda J, Hirai M, Toyoda A, Hashimoto K: Localization of the human transaldolase gene (TALDO) to chromosome 1p33→p34.1 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids. Genomics 40:378-381 (1997).
87. Lander ES, Green P: Construction of multi-locus genetic linkage maps in humans. Proc natl Acad Sci, USA 84:2363-2367 (1987).
88. Larsson C, Hellqvist M, Pierrou S, White I, Enerback S, Carlsson P: Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -6(FKHL10) and -8 (FKHL12). Genomics 30:464-469 (1995).
89. Lee WC, Balsara B, Liu Z, Jhanwar SC, Testa JR: Loss of heterozygosity analysis defines a critical region in chromosome 1p22 commonly deleted in human malignant mesothelioma. Cancer Res 56:4297-4301 (1996).
90. Lennon GG, Auffray C, Polymeropoulos M, Soares MB: The I.M.A.G.E. consortium: An integrated molecular analysis of genomes and their expression. Genomics 33:151-152 (1996).
91. Lesage F, Mattei M, Fink M, Barhanin J, Lazdunski M: Assignment of the human weak inward rectifier K+ channel TWIK-1 gene to chromosome lq42→ q43. Genomics 34:153-155 (1996).
92. Li YN, Gulati S, Baker PJ, Brody LC, Banerjee R, Kruger WD: Cloning, mapping and RNA analysis of the human methionine synthase gene. Hum Mol Genet 5:1851-1858 (1996).
93. Lin SW, Chen JC, Hsu LC, Hsieh CL, Yoshida A: Human gamma-aminobutyraldehyde dehydrogenase (ALDH9): cDNA sequence, genomic organization, polymorphism, chromosomal localization, and tissue expression. Genomics 34:376-380 (1996).
94. Lothe RA, Andersen SN, Hofstad B, Meling GI, Peltomaki P, Heim S, Brogger A, Vatn M, Rognum TO, Borresen A-L: Deletion of 1p loci and microsatellite instability in colorectal polyps. Genes Chrom Cancer 14:182-188 (1995).
95. Maestrini E, Monaco AP, McGrath JA, IshidaYamamoto A, Camisa C, Hovnanian A, Weeks DE, Lathrop M, Uitto J, Christiane AM: A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nature Genet 13:7077 (1996).
96. Maguchi M, Nishida W, Kohara K, Kuwano A, Kondo I, Hiwanda K: Molecular cloning and gene mapping of human basic and acidic calponins. Biochem biophys Res Comm 217:238-244 (1995).
97. Mahnke-Zizelman DK, van den Bergh F, Bausch Jurken MT, Eddy R, Sait S, Shows TB, Sabina RL: Cloning, sequence and characterization of the human AMPD2 gene: evidence for transcriptional regulation by two closely spaced promoters. Biochim biophys Acta 1308:122-132 (1996).
98. Makino Y, Ohga T, Toh S, Koike K, Okumura K, Wada M, Kuwano M, Kohno K: Structural and functional analysis of the human Y-box binding protein (YB-1) gene promoter. Nucl Acid Res 24:1873-1878 (1996).
99. Mancini M, Sala C, Rivella S, Toniolo D: Selection and fine mapping of chromosome-specific cDNAs: Application to human chromosome 1. Genomics 38:149-154 (1996).
100. Marenholz I, Volz A, Ziegler A, Davies A, Ragoussis I, Korge BP, Mischke D: Genetic analysis of the epidermal differentiation complex (EDC) on human chromosome 1q21 - chromosomal orientation, new markers, and a 6-Mb YAC contig. Genomics 37:295-302 (1996).
101. Maresco DL, Chang E, Theil KS, Francke U, Anderson CL: The three genes of the human FCGR1 gene family encoding Fc gamma RI flank the centromere of chromosome 1 at 1p12 and 1q21.Cytogenet Cell Genet 73:157-163 (1996).
102. Maris JM, Kyemba SM, Rebbeck TR, White PS, Sulman EP, Jensen SJ, Allen C, Biegel JA, Yanofsky RA, Feldman GL, Brodeur GM: Familial predisposition to neuroblastoma does not map to chromosome band 1p36. Cancer Res 56:3421-3425 (1996).
103. Mathew S, Murty W, Bosl GJ, Chaganti RS: Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Res 54:6265-6269 (1994).
104. Matise T, Perlin M, Chakravarti A: Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map. Nature Genet 6:384-390 (1994).
105. Matsuoka R, Sawamura T, Yamada K, Yoshida M, Furutani Y, Ikura T, Shiraki T, Hoshikawa H, Shimada K, Tanzawa K, Masaki T: Human endothelin converting enzyme gene (ECE1) mapped to chromosomal region 1p36.1. Cytogenet Cell Genet 72:322-324 (1996).
106. McCright B, Brothman AR, Virshup DM: Assignment of human protein phosphatase 2A regulatory subunit genes b56alpha, b56beta, b56gamma, b56delta, and b56epsilon (PPP2R5A-PPP2R5E), highly expressed in muscle and brain, to chromosome regions 1q41, 1q12, 3p21, 6p21.1, and 7p11.2p12. Genomics 36:168-170 (1996).
107. Meese E, Gotten E, Zang KD, Sauter M, Schommer S, Mueller-Lantzsch N: Human endogenous retroviral element k10 (HERV-K10): chromosomal localization by somatic hybrid mapping and fluorescence in situ hybridization. Cytogenet Cell Genet 72:40-42 (1996).
108. Mischke D, Korge BP, Marenholz I, Volz A, Ziegler A: Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex ("epidermal differentiation complex") on human chromosome 1q21. J Invest Dermatol 106:989-992 (1996).
109. Morton N: Parameters of the human genome. Proc natl Acad Sci, USA 88:7474-7476 (1991).
110. Muragaki Y, Mariman EC, van Beersum SE, Perala M, van Mourik JB, Warman ML, Olsen BR, Hamel BC: A mutation in the gene encoding the alpha 2 chain of the fibrilassociated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2). Nature Genet 12:103-105 (1996).
111. Munn KE, Walker RA, Varley JM: Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast. Oncogene 10:1653-1657 (1995).
112. Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J, Sheffield VC, Sunden S, Duyk GM, et al.: A comprehensive human linkage map with centimorgan density. Science 265:2049-2054 (1994).
113. Negus K, Holmes GH, Wicking C, Wainwright BJ, Little MH: +P5 (D1S3309E), a novel target binding site for the Wilms' tumour suppressor 1 (WT1) gene, maps to human chromosome 1q21→q22. Cytogenet Cell Genet 72:306-309 (1996).
114. Neri C, Albanese V, Lebre AS, Holbert S, Saada C, Bougueleret L, Meier-Ewert S, Le Gall I, Millasseau P, Bui H, Giudicelli C, Massart C, Guillou S, Gervy P, Poullier E, Rigault P, Weissenbach J, Lennon G, Chumakov I, Dausset J, Lehrach H, Cohen D, Cann HM: Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders. Hum Mol Genet 5:1001-1009 (1996).
115. Onyango P, Gardellin P, Lubyova B, Lummerstorfer JA, Paiha K, Ambros P, Biegel JA.Weith A: A high density physical map of a refined neuroblastoma consensus deletion at human chromosome 1p36.3. Abstract presented at this workshop (1997a).
116. Onyango P, Lubyova B, Gardellin P, Kurzbauer R, Weith A: Molecular cloning and expression analysis of five novel genes in chromosome 1p36. Abstract presented at this workshop (1997b).
117. Orlicky DJ, Berry R, Sikela JM: Human chromosome 1 localization of the gene for a prostaglandin F2 alpha receptor negative regulatory protein. Hum Genet 97:655-658 (1996).
118. Pardo-Manuel de Villena F, Heine-Suner D, Rodriguez de Cordoba S: Ordering of the human regulator of complement activation gene cluster on 1q32 by two-colour FISH. Cytogenet Cell Genet 72:339-341 (1996).
119. Pizzuti A, Amati F, Calabrese G, Mari A, Colosimo A, Silani V, Giardino L, Ratti A, Penso D, Calza L, Palka G, Scarlato G, Novelli G, Dallapiccola B: cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene. Hum Mol Genet 5:953-958 (1996).
120. Polymeropoulos MH, Ortiz De Luna RI, Ide SE, Torres R, Rubenstein J, Francomano CA: The gene for pycnodysostosis maps to human chromosome 1cen→q21. Nature Genet 10:238-239 (1995).
121. Praml C, Savelyeva L, Le Paslier D, Siracusa LD, Buchberg AM, Schwab, M, Amier LC: Human homologue of a candidate for the Mom 1 locus, the secretory type II phospholipase A2 (PLA2SII), maps to lp3536.1/D1S199. Cancer Res 55:5504-5506 (1995).
122. Praml C, Finke LH, Herfarth C, Schlag P, Schwab M, Amler LC: Deletion mapping defines different regions in 1p34.2→pter that may harbor genetic information relation to human colorectal cancer. Oncogene 11:1357-1362 (1995).
123. Rampazzo A, Nava A, Erne P, Eberhard M, Vian E, Slomp P, Tiso N, Thiene G, Danieli GA: A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42→ q43. Hum Mol Genet 4:2151-2154 (1995).
124. Reddy US, Phatak S, Allen C, Nycum LM, Sulman EP, White PS, Biegel JA: Localization of the human Ror 1 gene (NTRKR1) to chromosome 1 p31→p32 by fluorescence in situ hybridization and somatic cell hybrid analysis. Genomics 41:283-285 (1997).
125. Reynolds PA, Powlesland RM, Keen TJ, Inglehearn CF, Cunningham AF, Green ED, Brown KW: Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities. Genes Chrom Cancer 17:151-155 (1996).
126. Ribaudo MR, Di Leonardo A, Rubino P, Giallongo A, Feo S: Assignment of enolase processed pseudogene (ENO1P) to human chromosome 1 bands 1q41→q42. Cytogenet Cell Genet 74:201-202 (1996).
127. Roberts AG, Whatley SD, Daniels J, Holmans P, Fenton I, Owen MJ, Thompson P, Long C, Elder GH: Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23. Hum Mol Genet 4:2387-2390 (1995).
128. Robert T, Auffray C, Cowell JK: Regional localization of 192 genic markers on human chromosome 1. Genomics 36:337-340 (1996a).
129. Roberts T, Mead RS, Cowell JK: Characterisation of a human chromosome 1 somatic cell hybrid mapping panel and regional assignment of 6 novel STS. Ann hum Genet 60:213-220 (1996b).
130. Rozet JM, Gerber S, Perrault I, Camuzat A, Calvas P, Viegas-Pequignot E, Molina-Gomes D, Le Paslier D, Chumakov I, Munnich A: Structure and physical mapping of DR1, a TATA-binding protein-associated phosphoprotein gene to chromosome 1p22.1 and its exclusion in Stargardt disease (STGD). Genomics 36:554-556 (1996).
131. Saito-Ohara F, Uchida S, Takeuchi Y, Sasaki S, Hayashi A, Marumo F, Ikeuchi T: Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32→q33 by in situ hybridization. Genomics 36:372-374 (1996).
132. Sandrin MS, Henning MM, Lo MF, Baker E, Sutherland GR, McKenzie IF: Isolation and characterization of cDNA clones for Humly9: the human homologue of mouse Ly9. Immunogenetics 43:13-19 (1996).
133. Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tome' P, Aggarwal A, Bajorek E: A gene map of the human genome. Science 274:540-546 (1996).
134. Schultz D, Litt M, Smith L, Thayer M, McCormack K: Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B. Genomics 31:389-391 (1996).
135. Schwab M, Praml C, Amler LC: Genomic instability in 1p and human malignancies. Genes Chrom Cancer 16:211-229 (1996).
136. Schutte BC, Sander A, Malik M, Murray JC: Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32→q41. Genomics 36:507-514 (1996).
137. Shearman AM, Hudson TJ, Andresen JM, Wu X, Sohn RL, Haluska F, Housman DE, Weiss JS: The gene for Schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1→p36. Hum Mol Genet 5:1667-1672 (1996).
138. Sheffield VC, Stone EM, Alward WLM, Drack AV, Johnson AT, Streb LM, Nichols BE: Genetic linkage of familial open angle glaucoma to chromosome 1q21→q31. Nature Genet 4:4750 (1993).
139. Sheffield V, Weber J, Buetow K, Murray J, Even D, Wiles K, Gastier J, Pulido J, Yandava Y, Sunden S: A collection of tri-and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet 4:1837-1844 (1995).
140. Shi GP, Webb AC. Foster KE, Knoll JHM, Lemere CA, Munger JS, Chapman HA: Human cathepsin S: chromosomal localization, gene structure and tissue distribution. J biol Chem 269:11530-11536 (1994).
141. Sidhar SK, Clark J, Gill S, Hamoudi R, Crew AJ, Gwilliam R, Ross M, Linehan WM, Birdsall S, Shipley J, Cooper CS: The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene. Hum Mol Genet 5:1333-1338 (1996).
142. Sierra-Rivera E, Dasouki M, Summar ML, Krishnamani MRS, Meredith MJ, Rao PN, Phillips JA, Freeman ML: Assignment of the human gene (GLCLR) that encodes the regulatory subunit of gamma glutamylcysteine synthetase to chromosome 1p21. Cytogenet Cell Genet 72:252-254 (1996).
143. Sinha S, Maity SN, Seldin MF, de Crombrugghe B: Chromosomal assignment and tissue expression of CBF-C/NFY-C, the third subunit of the mammalian CCAAT-binding factor. Genomics 37:260-263 (1996).
144. Slupska MM, Baikalov C, Luther WM, Chiang JH, Wei YF, Miller JH: Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damage. J Bacteriol 178:3885-3892 (1996).
145. Smith JR, Freije D, Carpten JD, Gronberg H, Xu J, Isaacs SD, Brownstein MJ, Bova GS, Guo H, Bujnovszky P, Nusskern DR, Damber JE, Bergh A, Emanuelsson M, Kallioniemi OP, Walker-Daniels J, Bailey-Wilson JE, Beaty TH, Meyers DA, Walsh PC, Collins FS, Trent JM, Isaacs WB: Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search. Science 274:1371-1374 (1996).
146. Speleman F, Van-Camp G, Van-Roy N: Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization. Cytogenet Cell Genet 72:189-90 (1996).
147. Steiner G, Cairns P, Polascik TJ, Marshall FF, Epstein JI, Sidransky D, Schoenberg M: High-density mapping of chromosomal arm 1q in renal collecting duct carcinoma: Region of minimal deletion at 1q32.1→32.2. Cancer Res 56:5044-5046 (1996).
148. Stone EM, Fingert JH, Alward WLM, Nguyen TD, Polansky JR, Sunden SLF, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC: Identification of a gene that causes primary open angle glaucoma. Science 275:668-670 (1997).
149. Sulman EP, Dumanski J, White PS, Maris JM, Jensen SJ, Kyemba S, Zhao H, Brodeur GM: A common region of allelic loss at 1p31 in meningioma. Abstr.#2785. Proc AACR 38:416 (1997).
150. Sulman EP, Tang XX, Allen C, Biegel JA, Pleasure DE, Brodeur GM, Ikegaki N: ECK, a human EPH-related gene, maps to 1p36.1, a common region of alteration in human cancers. Genomics 40:371-374 (1997).
151. Sumegi J, Wang JY, Zhen DK, Eudy JD, Talmadge CB, Li BF, Berglund P, Weston MD, Yao SF, MaEdmonds M, Overbeck L, Kelley PM, Zabarovsky E, Uzvolgyi E, Stanbridge EJ, Klein G, Kimberling WJ: The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type Ha (USH2A) gene in 1q41. Genomics 35:79-86 (1996).
152. Sunden SLF, Alward WLM, Nichols BE, Rokhlina TR, Nystuen A, Stone EM, Sheffield VC: Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes. Genome Res 6:862-869 (1996).
153. Suzuki E, Lowry J, Sonoda G, Testa JR, Walsh K: Structures and chromosome locations of the human MEF2A gene and a pseudogene MEF2AP. Cytogenet Cell Genet 73:244-249 (1996).
154. Takano T, Sahara N, Yamanouchi Y, Mon H: Assignment of Alzheimer's presenilin-2 (PS-2) gene to 1q42.1 by fluorescence in situ hybridization. Neurosci Lett 221:205-207 (1997).
155. Taketani S, Inazawa J, Abe T, Furukawa T, Kohno H, Tokunaga R, Nishimura K, Inokuchi H: The human protoporphyrinogen oxidase gene (PPOX): organization and location to chromosome 1. Genomics 29:698-703 (1995).
156. Tamura N, Ogawa Y, Yasoda A, Itoh H, Saito Y, Nakao K: Two cardiac natriuretic peptide genes (atrial natriuretic peptide and brain natriuretic peptide) are organized in tandem in the mouse and human genomes. J Mol Cell Cardiol 28:1811-1815 (1996).
157. Tanaka K, Yanoshita R, Konishi M, Oshimura M, Maeda Y, Mod T, Miyaki M: Suppression of tumourigenicity in human colon carcinoma cells by introduction of normal chromosome 1p36 region. Oncogene 8:2253-2258 (1993).
158. Tsuchiya K, Mulcahy RT, Reid LL, Disteche CM, Kavanagh TJ: Mapping of the glutamate-cysteine ligase catalytic subunit gene (GLCLC) to human chromosome 6p12 and mouse chromosome 9D-E and of the regulatory subunit gene (GLCLR) to human chromosome 1p21→p22 and mouse chromosome 3H1-3. Genomics 30:630-632 (1995).
159. Tycko B, Smith SD, Sklar J: Chromosomal translocations joining LCK and TCRB loci in human T-cell leukemia. JexpMed 174:867-873 (1991).
160. Van Bokhoven H, Rawson RB, Merkx GFM, Cremers FPM, Seabra MC: cDNA cloning and chromosomal localization of the genes encoding the alpha and beta subunits of human Rab geranylgeranyl transferase: the 3′ end of the alpha subunit gene overlaps with the transglutaminase 1 gene promoter. Genomics 38:133-140 (1996).
161. Van der Drift P, Chan A, Laureys G, van roy N, Sickmann G, den Dunnen J, Westerveld A, Speleman F, Versteeg R: Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36. Genes Chrom Cancer 14:35-42 (1995).
162. Vocero-Akbani A, Helms C, Wang JC, Sanjurjo FJ, Korte-Sarfaty J, Veile RA, Liu L, Jauch A, Burgess AK, Hing AV, Holt MS, Ramachandra S, Whelan AJ, Anker R, Ahrent L, Chen M, Gavin MR, Iannantuoni K, Morton SM, Pandit SD, Read CM, Steinbrueck T, Warlick C, Smoller DA, Donis-Keller H: Mapping human telomere regions with YAC and PI clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions. Genomics 36:492-506 (1996).
163. Waldmann R, Bassilana F, Voilley N, Lazdunski M, Mattei MG: Assignment of the human amiloridesensitive Na(+) channel delta isoform to chromosome 1p36.3→p36.2. Genomics 34:262-263 (1996).
164. Walsh MT, Divane A, Whitehead AS: Fine mapping of the human pentraxin gene region on chromosome 1q23. Immunogenetics 44:62-69 (1996).
165. Walter MA, Spillett DJ, Thomas P, Weissenbach J, Goodfellow PN: A method for constructing radiation hybrid maps of whole genomes. Nature Genet 7:22-28 (1994).
166. Wang Y, Kudoh J, Kubota R, Asakawa S, Minoshima S, Shimizu N: Chromosomal mapping of a family of human glutamine synthetase genes: functional gene (GLUL) on 1q25, pseudogene (GLULP) on 9p13, and three related genes (GLULL1, GLULL2, GLULL3) on 5q33, 11q15, and 11q24. Genomics 37:195-199 (1996).
167. Watanabe TK, Kawai A, Fujiwara T, Maekawa H, Hirai Y, Nakamura Y, Takahashi E: Molecular cloning Of UBE2B, encoding a human skeletal muscle-specific ubiquitin-conjugating enzyme homologous to Ubc7 of C. elegans. Cytogenet Cell Genet 74:146-148 (1996).
168. Weier HU, George CX, Greulich KM, Samuel CE: The interferon-inducible. double-stranded RNA-specific adenosine deaminase gene (DSRAD) maps to human chromosome 1q21.1→21.2. Genomics 30:372-375 (1995).
169. Weith A, Brodeur G, Bruns G, Matise T. Mischke D, Nizetic D, Seldin M, van Roy N, Vance J: Report of the second international workshop on human chromosome 1 mapping 1995. Cytogenet Cell Genet 72:113-154 (1996).
170. White PS, Maris JM, Beltinger C, Sulman E, Marshall HN, Fujimori M, Kaufman BA, Biegel JA, Allen C, Hilliard C, Valentine MB, Look AT, Enomoto H, Sakiyama S, Brodeur GM: A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2→p36.3. Proc natl Acad Sci, USA 92:5520-5524 (1995).
171. Wicki R, Marenholz I, Mischke D, Schafer BW, Heizmann CW: Characterization of the human S100A12 (Calgranulin C, P6, CAAF1, CGRP) gene, a new member of the S100 gene cluster on chromosome 1q21. Cell Calcium 20:459-464 (1996a).
172. Wicki R, Schafer BW, Erne P, Heizmann CW: Characterization of the human and mouse cDNAs coding for S100A13, a new member of the S100 protein family. Biochem biophys Res Commun 227:594-599 (1996b).
173. Wiggs JL, Damji Kf, Haines JL, PericakVance MA, Allingham RR: The distinction between juvenile and adult-onset primary open-angle glaucoma [letter; comment]. Am J hum Genet 58:243-244 (1996).
174. Wiggs JL, Haines JL, Paglinauan C, Fine A, Sporn C, Lou D: Genetic linkage of autosomal dominant juvenile glaucoma to 1q21→q31 in three affected pedigrees. Genomics 21:299-303 (1994).
175. Wimmer K, Thoraval D, Asakawa J, Kuick R, Kodaira M, Lamb B, Fawcett J, Glover T, Cram S, Hanah S: Two-dimensional separation and cloning of chromosome 1 Not/I-EcoRV-derived genomic fragments. Genomics 38:124-132 (1996).
176. Wu HK, Heng HH, Shi XM, Forsdyke DR, Tsui LC, Mak TW, Mindon MD, Siderovski DP: Differential expression of a basic helix-loop-helix phosphoprotein gene, GOS8, in acute leukemia and localization to human chromosome 1q31. Leukemia 9:1291-1298.
177. Wydner KL, McNeil JA, Lin F, Worman HJ, Lawrence JB: Chromosomal assignment of human nuclear envelope protein genes LMNA, LMNB1 and LBR by fluorescence in-situ- hybridization. Genomics 32:474-478 (1996).
178. Xu SY, Schwartz M, Rosenberg T, Gal A: A ninth locus (RP18) for the autosomal dominant retinitis pigmentosa maps in the pericentric region of chromosome 1. Hum Mol Genet 5:1193-1197 (1996).
179. Yeh SH, Chen PJ, Chen HL, Lai MY, Wang CC, Chen DS: Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas. Cancer Res 54:4188-4192 (1994).
180. Zinovieva RD, Duncan MK, Johnson TR, Torres R, Polymeropoulos MH, Tomarev SI: Structure and chromosomal localization of the human homeobox gene PROX 1. Genomics 35:517-522 (1996).