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C Tsui

Showing results (351-360 of 453) with videos related to

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Medycyna Wieku Rozwojowego|October 3, 2000
[Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland]I Aznarez, J Bal, T Casals, et al.
Clinical Genetics|May 1, 1986
Linkage between the loci for cystic fibrosis and paraoxonaseK Schmiegelow, H Eiberg, L C Tsui, et al.
DNA and Cell Biology|June 1, 1997
Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1W F Dong, H H Heng, R Lowsky, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Human Genetics|April 1, 1998
Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I)T Onay, O Topaloglu, J Zielenski, et al.
Science (New York, N.Y.)|November 29, 1985
Cystic fibrosis locus defined by a genetically linked polymorphic DNA markerL C Tsui, M Buchwald, D Barker, et al.
Genomics|November 1, 1996
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotypeM Mackay, J Fantes, S Scherer, et al.
Oncogene|March 21, 1996
Identification of a human LIM-Hox gene, hLH-2, aberrantly expressed in chronic myelogenous leukaemia and located on 9q33-34.1H K Wu, H H Heng, D P Siderovski, et al.
Pageof 46

Showing results (351-360 of 453) with videos related to

Sort By:
Pageof 46
Medycyna Wieku Rozwojowego|October 3, 2000
[Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland]I Aznarez, J Bal, T Casals, et al.
Clinical Genetics|May 1, 1986
Linkage between the loci for cystic fibrosis and paraoxonaseK Schmiegelow, H Eiberg, L C Tsui, et al.
DNA and Cell Biology|June 1, 1997
Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1W F Dong, H H Heng, R Lowsky, et al.
Clinical Genetics|July 16, 2004
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.
Clinical Genetics|July 18, 2002
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)M Faiyaz-Ul-Haque, W Ahmad, S H E Zaidi, et al.
Human Genetics|April 1, 1998
Analysis of the CFTR gene in Turkish cystic fibrosis patients: identification of three novel mutations (3172delAC, P1013L and M1028I)T Onay, O Topaloglu, J Zielenski, et al.
Science (New York, N.Y.)|November 29, 1985
Cystic fibrosis locus defined by a genetically linked polymorphic DNA markerL C Tsui, M Buchwald, D Barker, et al.
Genomics|November 1, 1996
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotypeM Mackay, J Fantes, S Scherer, et al.
Oncogene|March 21, 1996
Identification of a human LIM-Hox gene, hLH-2, aberrantly expressed in chronic myelogenous leukaemia and located on 9q33-34.1H K Wu, H H Heng, D P Siderovski, et al.
Pageof 46