Volume 17; Issue 1

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Genomics
Volume 17; Issue 1

Genomics

Volume 17; Issue 1

1

A Radiation Hybrid Map of Human Chromosome 11q22-q23 Containing the Ataxia-Telangiectasia Disease Locus

Charles W. Richard III, David R. Cox, Leon Kapp, John Murnane, François Cornelis, Cecile Julier, G.Mark Lathrop, Michael R. James

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1993

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1993

2

G6PD Haplotypes Spanning Xq28 from F8C to Red/Green Color Vision

S. Filosa, V. Calabrò, G. Lania, T.J. Vulliamy, C. Brancati, A. Tagarelli, L. Luzzatto, G. Martini

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1993

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3

A Long-Range Restriction Map of Human Chromosome 5q21-q23

J.R.Tristan Ward, Sally Cottrell, Huw J.W. Thomas, Tania A. Jones, Cathy M. Howe, Garret M. Hampton, Larry Deaven, Denise Sheer, Walter F. Bodmer, Ellen Solomon, Anna-Maria Frischauf

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1993

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4

Physical Analysis of the Terminal 240 kb of DNA from Human Chromosome 7q

H.C. Riethman, C. Spais, J. Buckingham, D. Grady, R.K. Moyzis

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1993

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1993

5

Leukocyte Common Antigen-Related Phosphatase (LRP) Gene Structure: Conservation of the Genomic Organization of Transmembrane Protein Tyrosine Phosphatases

Edward C.C. Wong, Jerald E. Mullersman, Matthew L. Thomas

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1993

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6

Sequence-Tagged NotI Sites of Human Chromosome 21: Sequence Analysis and Mapping

Masahira Hattori, Atushi Toyoda, Hitoshi Ichikawa, Takashi Ito, Hideko Ohgusu, Nobue Oishi, Takeshi Kano, Satoru Kuhara, Misao Ohki, Yoshiyuki Sakaki

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1993

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1993

7

Structure and Expression of the Mouse Apolipoprotein C2 Gene

Mariëtte J.V. Hoffer, Marga M. van Eck, Louis M. Havekes, Marten H. Hofker, Rune R. Frants

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1993

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1993

8

YAC Clone Contigs Surrounding the Zfx and Pola Loci on the Mouse X Chromosome

Renata M.J. Hamvas, Zoia Larin, Neil Brockdorff, Sohaila Rastan, Hans Lehrach, Francois L. Chartier, Stephen D.M. Brown

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1993

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1993

9

Characterization and Sequence Analysis of Rat Serine:Pyruvate/Alanine:Glyoxylate Aminotransferase Gene

Toshiaki Oda, Kozo Nishiyama, Arata Ichiyama

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1993

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10

Genome Scanning of Human Breast Carcinomas Using Micro- and Minisatellite Core Probes

Eivind Hovig, Erik Mullaart, Anne-Lise Børresen, André G. Uitterlinden, Jan Vijg

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1993

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11

Molecular Cloning and Characterization of a Human Carboxylesterase Gene

Futoshi Shibata, Yasumitsu Takagi, Masato Kitajima, Toshihisa Kuroda, Tsuneo Omura

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1993

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1993

12

Analysis of Mdr50: A Drosophila P-Glycoprotein/Multidrug Resistance Gene Homolog

Bernard Gerrard, Claudia Stewart, Michael Dean

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1993

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1993

13

Molecular Basis and Consequences of a Deletion in the Amelogenin Gene, Analyzed by Capture PCR

Maria Lagerström-Fermér, Ulf Pettersson, Ulf Landegren

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1993

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14

Mapping of Glutamic Acid Decarboxylase (GAD) Genes

Susanne Edelhoff, Catherine E. Grubin, Allan E. Karlsen, David A. Adler, Don Foster, Christine M. Disteche, Åke Lernmark

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1993

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15

A Fluorescence in Situ Hybridization Map of Human Chromosome 21 Consisting of 30 Genetic and Physical Markers on the Chromosome: Localization of 137 Additional YAC and Cosmid Clones with Respect to This Map

Jeffrey C. Gingrich, Farideh Shadravan, Stephen R. Lowry

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1993

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16

Comparative Mapping of the Grpr Locus on the X Chromosomes of Man and Mouse

Gareth Ll. Maslen, Yvonne Boyd

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1993

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17

High-Resolution Comparative Mapping of Mouse Chromosome 17

Heinz Himmelbauer, Lee M. Silver

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1993

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1993

18

A Tetranucleotide Repeat Mouse Minisatellite Displaying Substantial Somatic Instability during Early Preimplantation Development

Mark Gibbs, Andrew Collick, Robert G. Kelly, Alec J. Jeffreys

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1993

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19

Colocalization of the Human CD59 Gene to 11p13 with the MIC11 Cell Surface Antigen

Wendy A. Bickmore, David Longbottom, Kathy Oghene, Judy U. Fletcher, Veronica van Heyningen

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1993

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1993

20

Molecular Analysis of Phenylketonuria in Denmark: 99% of the Mutations Detected by Denaturing Gradient Gel Electrophoresis

Per Guldberg, Karen Friis Henriksen, Flemming Güttler

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1993

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21

Physical Mapping of DNA Markers in the q13-q22 Region of the Human X Chromosome

Christophe Philippe, Frans P.M. Cremers, Michèle Chery, Irène Bach, Naı̈ma Abbadi, H.Hilger Ropers, Simone Gilgenkrantz

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1993

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1993

22

High-Resolution Cytogenetic Mapping of 342 New Cosmid Markers Including 43 RFLP Markers on Human Chromosome 17 by Fluorescence in Situ Hybridization

Johji Inazawa, Hiroko Saito, Takeshi Ariyama, Tatsuo Abe, Yusuke Nakamura

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1993

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1993

23

High-Resolution Mapping of Probes near the X-Linked Lymphoproliferative Disease (XLP) Locus

Bai-Lin Wu, Aubrey Milunsky, David Nelson, Barbara Schmeckpeper, Giovanni Porta, David Schlessinger, James Skare

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1993

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24

Mitochondrial DNA Variants Observed in Alzheimer Disease and Parkinson Disease Patients

John M. Shoffner, Michael D. Brown, Antonio Torroni, Marie T. Lott, Margaret F. Cabell, Suzanne S. Mirra, M.Flint Beal, Chi-Chuan Yang, Marla Gearing, Rino Salvo, Ray L. Watts, Jorge L. Juncos, Lawren

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1993

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25

C4BPAL1, a Member of the Human Regulator of Complement Activation (RCA) Gene Cluster That Resulted from the Duplication of the Gene Coding for the α-Chain of C4b-Binding Protein

Pilar Sánchez-Corral, Fernando Pardo-Manuel de Villena, Javier Rey-Campos, Santiago Rodrı́guez de Córdoba

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1993

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1993

26

Nucleotide Sequence, Expression, and Chromosomal Mapping of Mrp and Mapping of Five Related Sequences

David F. Lobach, Julie M. Rochelle, Mark L. Watson, Michael F. Seldin, Perry J. Blackshear

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1993

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27

Multipoint Mapping of the Central Core Disease Locus

S. Schwemmle, K. Wolff, L.M. Palmucci, T. Grimm, F. Lehmann-Horn, Ch. Hübner, E. Hauser, D.E. Iles, D.H. MacLennan, C.R. Müller

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1993

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28

Isolation and Characterization of Three Microsatellite Markers in the Proximal Long Arm of the Human X Chromosome

S. Lindsay, A.R.J. Curtis, P. Roustan, S. Kamakari, D.L. Thiselton, A. Stephenson, S.S. Bhattacharya

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1993

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29

Fifty Sequenced-Tagged Sites on Human Chromosome 11

Tokiko Miwa, Kazunori Sudo, Yusuke Nakamura, Takashi Imai

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1993

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30

A Homoallelic Gly317 → Asp Mutation in ALPL Causes the Perinatal (Lethal) Form of Hypophosphatasia in Canadian Mennonites

Cheryl R. Greenberg, Cheryl L.D. Taylor, James C. Haworth, Lorne E. Seargeant, Sylvia Philipps, Barbara Triggs-Raine, Bernard N. Chodirker

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1993

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31

A Fourth Example Suggests That Premature Termination Codons in the COL2A1 Gene Are a Common Cause of the Stickler Syndrome: Analysis of the COL2A1 Gene by Denaturing Gradient Gel Electrophoresis

Pertti Ritvaniemi, James Hyland, Jaakko Ignatius, Kari I. Kivirikko, Darwin J. Prockop, Leena Ala-Kokko

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1993

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32

Assignment of the Nuclear Mitotic Apparatus Protein NuMA Gene to Human Chromosome 11q13

Cynthia A. Sparks, Peter L. Bangs, Gerard P. McNeil, Jeanne B. Lawrence, Edward G. Fey

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1993

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33

Sequence and Characterization of the Complete Human Thrombospondin 2 cDNA: Potential Regulatory Role for the 3′ Untranslated Region

Terry L. Labell, Peter H. Byers

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1993

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34

Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa

S. Bunge, H. Wedemann, D. David, D.J. Terwilliger, L.I. van den Born, C. Aulehla-Scholz, C. Samanns, M. Horn, J. Ott, E. Schwinger, A. Schinzel, M.J. Denton, A. Gal

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1993

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35

A High-Resolution Cytogenetic Map of Human Chromosome 5: Localization of 206 New Cosmid Markers by Direct R-Banding Fluorescence in Situ Hybridization

Ei-ichi Takahashi, Akitsu Hitomi, Yusuke Nakamura

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1993

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1993

36

Mapping of the Human NMDA Receptor Subunit (NMDAR1) and the Proposed NMDA Receptor Glutamate-Binding Subunit (NMDARA1) to Chromosomes 9q34.3 and Chromosome 8, Respectively

Colin Collins, Catherine Duff, Alessandra M.V. Duncan, Rosa Planells-Cases, William Sun, Anne Norremolle, Elias Michaelis, Mauricio Montal, Ronald Worton, Michael R. Hayden

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1993

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37

Mapping of the Human CENP-B Gene to Chromosome 20 and the CENP-C Gene to Chromosome 12 by a Rapid Cycle DNA Amplification Procedure

Kenji Sugimoto, Hiroaki Yata, Michio Himeno

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1993

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38

Molecular Characterization of an Intragenic Minisatellite (VNTR) Polymorphism in the Human Parathyroid Hormone-Related Peptide Gene in Chromosome Region 12p12.1-p11.2

Zdenka Pausova, Kenneth Morgan, T.Mary Fujiwara, Johanne Bourdon, David Goltzman, Geoffrey N. Hendy

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1993

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1993

39

A Continuous Linkage Map of 22 Short Tandem Repeat Polymorphisms on Human Chromosome 12

Elisabeth Dawson, Sanober Shaikh, James L. Weber, Zhenyuan Wang, Jean Weissenbach, John F. Powell, Michael Gill

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1993

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40

The Human Paired Domain Gene PAX7 (Hup1) Maps to Chromosome 1p35-1p36.2

B.W. Schäfer, M.G. Mattei

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1993

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41

Assignment of the Chromogranin A (Chga) Locus to Homologous Regions on Mouse Chromosome 12 and Rat Chromosome 6

Dominique Simon-Chazottes, Hongjiang Wu, Robert J. Parmer, David J. Rozansky, Josiane Szpirer, Goran Levan, Theodore W. Kurtz, Claude Szpirer, Jean Louis Guenet, Daniel T. O'Connor

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1993

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42

D21S418E Identifies a cAMP-Regulated Gene Located on Chromosome 21q22.3 That Is Expressed in Placental Syncytiotrophoblast and Choriocarcinoma Cells

Susumu Kido, Noriaki Sakuragi, Mary P. Bronner, Raja Sayegh, Ralph Berger, David Patterson, Jerome F. Strauss III

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1993

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43

Demonstration of Physical Linkage between the Promoter Region and the Polymorphic Kringle IV Domain in the Apo(a) Gene by Pulsed-Field Gel Electrophoresis

H.G. Kraft, N. Malgaretti, S. Köchl, F. Acquati, G. Utermann, R. Taramelli

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1993

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1993

44

Localization of Human Indoleamine 2,3-Dioxygenase (IDO) Gene to the Pericentromeric Region of Human Chromosome 8

Dean J. Burkin, K.Sean Kimbro, Barbara L. Barr, Carol Jones, Milton W. Taylor, Sohan L. Gupta

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1993

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45

Localization of the Estrogen Receptor Locus (ESR) to Chromosome 6q25.1 by FISH and a Simple Post-FISH Banding Technique

L.P. Menasce, G.R.M. White, C.J. Harrison, J.M. Boyle

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1993

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46

The Genes for Oncostatin M (OSM) and Leukemia Inhibitory Factor (LIF) Are Tightly Linked on Human Chromosome 22

Timothy M. Rose, Michelle J. Lagrou, Ingegerd Fransson, Barbro Werelius, Olivier Delattre, Gilles Thomas, Pieter J. de Jong, George J. Todaro, Jan P. Dumanski

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1993

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1993

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