A Hajra|F S Collins - JoVE Visualize

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Nucleic Acids Research|February 25, 1989

Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomesM R Wallace, J W Fountain, A M Brereton, et al.

Genes, Chromosomes & Cancer|April 1, 1993

The human NME2 gene lies within 18kb of NME1 in chromosome 17S C Chandrasekharappa, L A Gross, S E King, et al.

Pediatrics|October 1, 1987

Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspectsJ H Seashore, F S Collins, R I Markowitz, et al.

Science (New York, N.Y.)|October 4, 1991

A bacterial system for investigating transport effects of cystic fibrosis--associated mutationsA L Gibson, L M Wagner, F S Collins, et al.

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.

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.

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.

Pageof 24

Showing results (61-70 of 234) with videos related to

Sort By:

Pageof 24

Nucleic Acids Research|February 25, 1989

Direct construction of a chromosome-specific NotI linking library from flow-sorted chromosomesM R Wallace, J W Fountain, A M Brereton, et al.

Genes, Chromosomes & Cancer|April 1, 1993

The human NME2 gene lies within 18kb of NME1 in chromosome 17S C Chandrasekharappa, L A Gross, S E King, et al.

Pediatrics|October 1, 1987

Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspectsJ H Seashore, F S Collins, R I Markowitz, et al.

Science (New York, N.Y.)|October 4, 1991

A bacterial system for investigating transport effects of cystic fibrosis--associated mutationsA L Gibson, L M Wagner, F S Collins, et al.

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.

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.

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.

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