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Blood|July 1, 1995

Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhoodK Stegmaier, S Pendse, G F Barker, et al.

Cytogenetics and Cell Genetics|January 1, 1995

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21A L George, T A Varkony, H A Drabkin, et al.

Investigative Ophthalmology|June 1, 1976

Successful therapy of herpes hominis keratitis in rabbits by 5-iodo-5'-amino-2'5'-dideoxyuridine (AIU): a novel analog of thymidineD M Albert, M Lahav, P N Bhatt, et al.

Genomics|October 1, 1990

Genetic and physical mapping and population studies of a fibronectin receptor beta-subunit-like sequence on human chromosome 19L A Giuffra, P Lichter, J S Wu, et al.

Genomics|July 15, 1994

A YAC contig spanning a cluster of human type III receptor protein tyrosine kinase genes (PDGFRA-KIT-KDR) in chromosome segment 4q12R A Spritz, K M Strunk, S T Lee, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995

Emergence of the ZNF91 Krüppel-associated box-containing zinc finger gene family in the last common ancestor of anthropoideaE J Bellefroid, J C Marine, A G Matera, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 23, 1995

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemiaT R Golub, G F Barker, S K Bohlander, et al.

Bioorganic & Medicinal Chemistry Letters|December 1, 2006

Synthesis and SAR of novel 2-arylthiazolidinones as selective analgesic N-type calcium channel blockersLars J S Knutsen, Christopher J Hobbs, Christopher G Earnshaw, et al.

Journal of the American Medical Informatics Association : JAMIA|November 1, 1995

Internet-based support for bioscience research: a collaborative genome center for human chromosome 12P L Miller, P M Nadkarni, K K Kidd, et al.

Human Molecular Genetics|February 1, 1996

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21U Schell, J Wienberg, A Köhler, et al.

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Showing results (211-220 of 221) with videos related to

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Pageof 23

Blood|July 1, 1995

Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhoodK Stegmaier, S Pendse, G F Barker, et al.

Cytogenetics and Cell Genetics|January 1, 1995

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21A L George, T A Varkony, H A Drabkin, et al.

Investigative Ophthalmology|June 1, 1976

Successful therapy of herpes hominis keratitis in rabbits by 5-iodo-5'-amino-2'5'-dideoxyuridine (AIU): a novel analog of thymidineD M Albert, M Lahav, P N Bhatt, et al.

Genomics|October 1, 1990

Genetic and physical mapping and population studies of a fibronectin receptor beta-subunit-like sequence on human chromosome 19L A Giuffra, P Lichter, J S Wu, et al.

Genomics|July 15, 1994

A YAC contig spanning a cluster of human type III receptor protein tyrosine kinase genes (PDGFRA-KIT-KDR) in chromosome segment 4q12R A Spritz, K M Strunk, S T Lee, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995

Emergence of the ZNF91 Krüppel-associated box-containing zinc finger gene family in the last common ancestor of anthropoideaE J Bellefroid, J C Marine, A G Matera, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 23, 1995

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemiaT R Golub, G F Barker, S K Bohlander, et al.

Bioorganic & Medicinal Chemistry Letters|December 1, 2006

Synthesis and SAR of novel 2-arylthiazolidinones as selective analgesic N-type calcium channel blockersLars J S Knutsen, Christopher J Hobbs, Christopher G Earnshaw, et al.

Journal of the American Medical Informatics Association : JAMIA|November 1, 1995

Internet-based support for bioscience research: a collaborative genome center for human chromosome 12P L Miller, P M Nadkarni, K K Kidd, et al.

Human Molecular Genetics|February 1, 1996

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21U Schell, J Wienberg, A Köhler, et al.

Pageof 23