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F S Collins

Showing results (101-110 of 297) with videos related to

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Blood|December 1, 1987
The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobasesF S Collins, J L Cole, W K Lockwood, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1994
Acute myeloid leukemia with Inv (16) produces a chimeric transcription factor with a myosin heavy chain tailP Liu, N Seidel, D Bodine, et al.
Science (New York, N.Y.)|October 23, 1998
New goals for the U.S. Human Genome Project: 1998-2003F S Collins, A Patrinos, E Jordan, et al.
The American Review of Respiratory Disease|October 1, 1988
The introduction of biologically active foreign genes into human respiratory epithelial cells using electroporationM C Iannuzzi, J L Weber, J Yankaskas, et al.
Cell|September 8, 1995
TEL1, an S. cerevisiae homolog of the human gene mutated in ataxia telangiectasia, is functionally related to the yeast checkpoint gene MEC1D M Morrow, D A Tagle, Y Shiloh, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 1997
Characterization of the CHD family of proteinsT Woodage, M A Basrai, A D Baxevanis, et al.
Cambridge Quarterly of Healthcare Ethics : CQ : the International Journal of Healthcare Ethics Committees|January 1, 1995
Case: responding to a request for genetic testing that is still in the labL G Biesecker, F S Collins, E G DeRenzo, et al.
Human Molecular Genetics|July 1, 1993
An alternatively-spliced mRNA in the carboxy terminus of the neurofibromatosis type 1 (NF1) gene is expressed in muscleD H Gutman, L B Andersen, J L Cole, et al.
Oncogene|March 1, 1993
Analysis of the neurofibromatosis type 1 (NF1) GAP-related domain by site-directed mutagenesisD H Gutmann, M Boguski, D Marchuk, et al.
The EMBO Journal|October 1, 1986
Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intronJ E Metherall, F S Collins, J Pan, et al.
Pageof 30

Showing results (101-110 of 297) with videos related to

Sort By:
Pageof 30
Blood|December 1, 1987
The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobasesF S Collins, J L Cole, W K Lockwood, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1994
Acute myeloid leukemia with Inv (16) produces a chimeric transcription factor with a myosin heavy chain tailP Liu, N Seidel, D Bodine, et al.
Science (New York, N.Y.)|October 23, 1998
New goals for the U.S. Human Genome Project: 1998-2003F S Collins, A Patrinos, E Jordan, et al.
The American Review of Respiratory Disease|October 1, 1988
The introduction of biologically active foreign genes into human respiratory epithelial cells using electroporationM C Iannuzzi, J L Weber, J Yankaskas, et al.
Cell|September 8, 1995
TEL1, an S. cerevisiae homolog of the human gene mutated in ataxia telangiectasia, is functionally related to the yeast checkpoint gene MEC1D M Morrow, D A Tagle, Y Shiloh, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 1997
Characterization of the CHD family of proteinsT Woodage, M A Basrai, A D Baxevanis, et al.
Cambridge Quarterly of Healthcare Ethics : CQ : the International Journal of Healthcare Ethics Committees|January 1, 1995
Case: responding to a request for genetic testing that is still in the labL G Biesecker, F S Collins, E G DeRenzo, et al.
Human Molecular Genetics|July 1, 1993
An alternatively-spliced mRNA in the carboxy terminus of the neurofibromatosis type 1 (NF1) gene is expressed in muscleD H Gutman, L B Andersen, J L Cole, et al.
Oncogene|March 1, 1993
Analysis of the neurofibromatosis type 1 (NF1) GAP-related domain by site-directed mutagenesisD H Gutmann, M Boguski, D Marchuk, et al.
The EMBO Journal|October 1, 1986
Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intronJ E Metherall, F S Collins, J Pan, et al.
Pageof 30