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L M Mulligan

Showing results (31-40 of 80) with videos related to

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American Journal of Medical Genetics|October 15, 1994
Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindredE Dow, S Cross, D J Wolgemuth, et al.
British Journal of Cancer|July 17, 1999
Mutation and deletion analysis of GFR alpha-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumoursO Gimm, A Gössling, D J Marsh, et al.
Cytogenetics and Cell Genetics|June 14, 2002
Conservation of RET proto-oncogene splicing variants and implications for RET isoform functionM T Carter, J L Yome, M N Marcil, et al.
Human Genetics|June 21, 2001
Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung diseaseJ B Vanhorne, O Gimm, S M Myers, et al.
Oncogene|March 3, 1998
Genomic structure and chromosomal localization of the human GDNFR-alpha geneC Eng, S M Myers, M D Kogon, et al.
Human Genetics|November 1, 1994
A novel polymorphism in the coding sequence of the human RET proto-oncogeneP Edery, T Attié, L M Mulligan, et al.
Journal of Medical Genetics|April 16, 1999
Investigation of germline GFR alpha-1 mutations in Hirschsprung diseaseS M Myers, R Salomon, A Goessling, et al.
British Journal of Cancer|August 1, 1996
Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytomaC Eng, K A Foster, C S Healey, et al.
Human Molecular Genetics|October 1, 1994
Haplotype analysis of MEN 2 mutationsE Gardner, L M Mulligan, C Eng, et al.
Journal of Neurogenetics|June 1, 1985
The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implicationsC J Forster-Gibson, L M Mulligan, M W Partington, et al.
Pageof 8

Showing results (31-40 of 80) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics|October 15, 1994
Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindredE Dow, S Cross, D J Wolgemuth, et al.
British Journal of Cancer|July 17, 1999
Mutation and deletion analysis of GFR alpha-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumoursO Gimm, A Gössling, D J Marsh, et al.
Cytogenetics and Cell Genetics|June 14, 2002
Conservation of RET proto-oncogene splicing variants and implications for RET isoform functionM T Carter, J L Yome, M N Marcil, et al.
Human Genetics|June 21, 2001
Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung diseaseJ B Vanhorne, O Gimm, S M Myers, et al.
Oncogene|March 3, 1998
Genomic structure and chromosomal localization of the human GDNFR-alpha geneC Eng, S M Myers, M D Kogon, et al.
Human Genetics|November 1, 1994
A novel polymorphism in the coding sequence of the human RET proto-oncogeneP Edery, T Attié, L M Mulligan, et al.
Journal of Medical Genetics|April 16, 1999
Investigation of germline GFR alpha-1 mutations in Hirschsprung diseaseS M Myers, R Salomon, A Goessling, et al.
British Journal of Cancer|August 1, 1996
Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytomaC Eng, K A Foster, C S Healey, et al.
Human Molecular Genetics|October 1, 1994
Haplotype analysis of MEN 2 mutationsE Gardner, L M Mulligan, C Eng, et al.
Journal of Neurogenetics|June 1, 1985
The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implicationsC J Forster-Gibson, L M Mulligan, M W Partington, et al.
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