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American Journal of Medical Genetics
|
October 15, 1994
Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindred
E 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 tumours
O 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 function
M 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 disease
J B Vanhorne, O Gimm, S M Myers, et al.
Oncogene
|
March 3, 1998
Genomic structure and chromosomal localization of the human GDNFR-alpha gene
C 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-oncogene
P Edery, T Attié, L M Mulligan, et al.
Journal of Medical Genetics
|
April 16, 1999
Investigation of germline GFR alpha-1 mutations in Hirschsprung disease
S 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 phaeochromocytoma
C Eng, K A Foster, C S Healey, et al.
Human Molecular Genetics
|
October 1, 1994
Haplotype analysis of MEN 2 mutations
E 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 implications
C J Forster-Gibson, L M Mulligan, M W Partington, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 80) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics
|
October 15, 1994
Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindred
E 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 tumours
O 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 function
M 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 disease
J B Vanhorne, O Gimm, S M Myers, et al.
Oncogene
|
March 3, 1998
Genomic structure and chromosomal localization of the human GDNFR-alpha gene
C 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-oncogene
P Edery, T Attié, L M Mulligan, et al.
Journal of Medical Genetics
|
April 16, 1999
Investigation of germline GFR alpha-1 mutations in Hirschsprung disease
S 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 phaeochromocytoma
C Eng, K A Foster, C S Healey, et al.
Human Molecular Genetics
|
October 1, 1994
Haplotype analysis of MEN 2 mutations
E 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 implications
C J Forster-Gibson, L M Mulligan, M W Partington, et al.
Page
of 8