Menu

Identification of Imprinted Loci by Methylation-Sensitive Representational Difference Analysis: Application to Mouse Distal Chromosome 2

By Kelsey G., Bodle D., Miller H.J., Beechey C.V., Coombes C., Peters J., Williamson C.M. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

A 2-Mb Sequence-Ready Contig Map and a Novel Immunoglobulin Superfamily Gene IGSF4 in the LOH Region of Chromosome 11q23.2

By Gomyo H., Arai Y., Tanigami A., Murakami Y., Hattori M., Hosoda F., Arai K., Aikawa Y., Tsuda H., Hirohashi S., Asakawa S., Shimizu N., Soeda E., Sakaki Y., Ohki M. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

A 1-Mb PAC Contig Spanning the Common Eliminated Region 1 (CER1) in Microcell Hybrid-Derived SCID Tumors

By Yang Y., Kiss H., Kost-Alimova M., Kedra D., Fransson I., Seroussi E., Li J., Szeles A., Kholodnyuk I., Imreh M.P., Fodor K., Hadlaczky G., Klein G., Dumanski J.P., Imreh S. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11

By Engert J.C., Dore C., Mercier J., Ge B., Betard C., Rioux J.D., Owen C., Berube P., Devon K., Birren B., Melancon S.B., Morgan K., Hudson T.J., Richter A. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

High-Level Expression of the Mnb/Dyrk1A Gene in Brain and Heart during Rat Early Development

By Okui M., Ide T., Morita K., Funakoshi E., Ito F., Ogita K., Yoneda Y., Kudoh J., Shimizu N. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

Human Connexin 30 (GJB6), a Candidate Gene for Nonsyndromic Hearing Loss: Molecular Cloning, Tissue-Specific Expression, and Assignment to Chromosome 13q12

By Kelley P.M., Abe S., Askew J.W., Smith S.D., Usami S.-i., Kimberling W.J. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

Physical Map and Characterization of Transcripts in the Candidate Interval for Familial Chondrocalcinosis at Chromosome 5p15.1

By Rojas K., Serrano de la Pena L., Gallardo T., Simmons A., Nyce K., McGrath R., Considine E., Vasko A.J., Peterson E., Grady D., Cox R., Andrew L.J., Lovett M., Overhauser J., Williams C.J. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

Homozygous Deletions Define a Region of 8p23.2 Containing a Putative Tumor Suppressor Gene

By Sun P.C., Schmidt A.P., Pashia M.E., Sunwoo J.B., Scholnick S.B. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

A Complete Comparative Chromosome Map for the Dog, Red Fox, and Human and Its Integration with Canine Genetic Maps

By Yang F., O'Brien P.C.M., Milne B.S., Graphodatsky A.S., Solanky N., Trifonov V., Rens W., Sargan D., Ferguson-Smith M.A. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite

Frequent Sequence Variation in the Human Myostatin (GDF8) Gene as a Marker for Analysis of Muscle-Related Phenotypes

By Ferrell R.E., Conte V., Lawrence E.C., Roth S.M., Hagberg J.M., Hurley B.F. in (1999)

Elsevier

Abstract Access to resources Recommend Favorite