Genomics

Isolation of a Gene (DLG3) Encoding a Second Member of the Discs-Large Family on Chromosome 17q12-q21
pp. 145-150(6)
Authors: Smith S.A.; Holik P.; Stevens J.; Mazoyer S.; Melis R.; Williams B.; White R.; Albertsen H.

Mouse Annexin V Chromosomal Localization, cDNA Sequence Conservation, and Molecular Evolution
pp. 151-157(7)
Authors: Rodriguez-Garcia M.I.; Kozak C.A.; Morgan R.O.; Fernandez M.P.

Maternal-Specific Methylation of the Human IGF2R Gene Is Not Accompanied by Allele-Specific Transcription
pp. 158-166(9)
Authors: Riesewijk A.M.; Schepens M.T.; Welch T.R.; van den Berg-Loonen E.M.; Mariman E.M.; Ropers H.H.; Kalscheuer V.M.

Human ESP1/CRP2, a Member of the LIM Domain Protein Family: Characterization of the cDNA and Assignment of the Gene Locus to Chromosome 14q32.3
pp. 167-176(10)
Authors: Karim M.A.; Ohta K.; Egashira M.; Jinno Y.; Niikawa N.; Matsuda I.; Indo Y.

Sequence Analysis, Chromosomal Location, and Developmental Expression of the Mouse Preproendothelin-1 Gene
pp. 177-184(8)
Authors: Maemura K.; Kurihara H.; Kurihara Y.; Oda H.; Ishikawa T.; Copeland N.G.; Gilbert D.J.; Jenkins N.A.; Yazaki Y.

Rapid Restriction Mapping of Cosmids by Sequence-Specific Triple-Helix-Mediated Affinity Capture
pp. 185-192(8)
Authors: Ji H.; Francisco T.; Smith L.M.; Guilfoyle R.A.

Detection of a Megabase Deletion in a Patient with Branchio-Oto-Renal Syndrome (BOR) and Tricho-Rhino-Phalangeal Syndrome (TRPS): Implications for Mapping and Cloning the BOR Gene
pp. 201-206(6)
Authors: Gu J.Z.; Wagner M.J.; Haan E.A.; Wells D.E.

Genomic Characterization of Human HMGIC, a Member of the Accessory Transcription Factor Family Found at Translocation Breakpoints in Lipomas
pp. 207-214(8)
Authors: Ashar H.R.; Cherath L.; Przybysz K.M.; Chada K.

Genes in a 220-kb Region Spanning the TNF Cluster in Human MHC
pp. 215-222(8)
Authors: Nalabolu S.R.; Shukla H.; Nallur G.; Parimoo S.; Weissman S.M.

Complete Genomic Organization of the Human Erythroid p55 Gene (MPP1), a Membrane-Associated Guanylate Kinase Homologue
pp. 223-229(7)
Authors: Kim A.C.; Metzenberg A.B.; Sahr K.E.; Marfatia S.M.; Chishti A.H.

Localization of Two Metabotropic Glutamate Receptor Genes, GRM3 and GRM8 , to Human Chromosome 7q
pp. 230-233(4)
Authors: Scherer S.W.; Duvoisin R.M.; Kuhn R.; Heng H.H.Q.; Belloni E.; Tsui L.C.

Physical and Genetic Localization of the Gene Encoding the AP-2 Transcription Factor to Mouse Chromosome 13
pp. 234-237(4)
Authors: Warren G.; Gordon M.; Siracusa L.D.; Buchberg A.M.; Williams T.

Chromosomal Assignment of the Gene Encoding the Human 58-kDa Inhibitor (PRKRI) of the Interferon-Induced dsRNA-Activated Protein Kinase to Chromosome 13q32
pp. 238-239(2)
Authors: Korth M.J.; Edelhoff S.; Disteche C.M.; Katze M.G.

PTPN13, a Fas-Associated Protein Tyrosine Phosphatase, Is Located on the Long Arm of Chromosome 4 at Band q21.3
pp. 240-242(3)
Authors: Inazawa J.; Ariyama T.; Abe T.; Druck T.; Ohta M.; Huebner K.; Yanagisawa J.; Reed J.C.; Sato T.

Molecular Cloning and Chromosomal Localization of the ADH7 Gene Encoding Human Class IV (sigma) ADH
pp. 243-245(1)
Authors: Yokoyama H.; Baraona E.; Lieber C.S.

Human Endopeptidase (THOP1) Is Localized on Chromosome 19 within the Linkage Region for the Late-Onset Alzheimer Disease AD2 Locus
pp. 246-249(4)
Authors: Meckelein B.; de Silva H.A.R.; Roses A.D.; Rao P.N.; Pettenati M.J.; Xu P.T.; Hodge R.; Glucksman M.J.; Abraham C.R.

The Bona Fide Mouse U7 snRNA Gene Maps to a Different Chromosome Than Two U7 Pseudogenes
pp. 250-252(3)
Authors: Turner P.C.; Whalen A.; Schumperli D.; Matera A.G.

Fine Mapping of the Human and Mouse Genes for the Type I Procollagen COOH-Terminal Proteinase Enhancer Protein
pp. 253-256(4)
Authors: Takahara K.; Osborne L.; Elliott R.W.; Tsui L.C.; Scherer S.W.; Greenspan D.S.

The Gene for Calcium-Modulating Cyclophilin Ligand (CAMLG) Is Located on Human Chromosome 5q23 and a Syntenic Region of Mouse Chromosome 13
pp. 257-260(4)
Authors: Bram R.J.; Valentine V.; Shapiro D.N.; Jenkins N.A.; Gilbert D.J.; Copeland N.G.

Mouse Chromosomal Location of Four Na/H Exchanger Isoform Genes
pp. 261-263(3)
Authors: Pathak B.G.; Shull G.E.; Jenkins N.A.; Copeland N.G.

Mapping of the Human HMG2 Gene to 4q31
pp. 264-265(2)
Authors: Wanschura S.; Schoenmakers E.F.P.M.; Huysmans C.; Bartnitzke S.; de Ven W.J.M.V.; Bullerdiek J.

Detection of a Large RIII-Derived Chromosomal Segment on Chromosome 10 in the H-2 Congenic Strain B10.RIII(71NS)/Sn
pp. 266-269(4)
Authors: Dong P.; Hood L.; McIndoe R.A.