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Genes, Chromosomes & Cancer
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March 1, 1993
Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2
L M Mulligan, E Gardner, B A Smith, et al.
Oncogene
|
May 15, 1998
Analysis of PTEN and the 10q23 region in primary prostate carcinomas
H E Feilotter, M A Nagai, A H Boag, et al.
Human Molecular Genetics
|
March 1, 1993
Localisation of the gene for multiple endocrine neoplasia type 2A to a 480 kb region in chromosome band 10q11.2
S E Mole, L M Mulligan, C S Healey, et al.
Oncogene
|
September 1, 1993
Structural analysis of the human ret proto-oncogene using exon trapping
J B Kwok, E Gardner, J P Warner, et al.
American Journal of Medical Genetics
|
January 1, 1986
An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis
C J Forster-Gibson, L M Mulligan, N E Simpson, et al.
Clinical Genetics
|
February 1, 1997
Mutation of RET codon 768 is associated with the FMTC phenotype
L M Boccia, J S Green, C Joyce, et al.
Cancer Research
|
January 15, 1997
Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas
P L Dahia, S P Toledo, L M Mulligan, et al.
Journal of Medical Genetics
|
September 9, 2000
Characterisation of the human GFRalpha-3 locus and investigation of the gene in Hirschsprung disease
C I Onochie, L M Korngut, J B Vanhorne, et al.
Surgery
|
December 1, 1994
Clinical value of direct DNA analysis of the RET proto-oncogene in families with multiple endocrine neoplasia type 2A
G L Feldman, M Kambouris, G B Talpos, et al.
Oncogene
|
May 22, 2001
Over-representation of a germline variant in the gene encoding RET co-receptor GFRalpha-1 but not GFRalpha-2 or GFRalpha-3 in cases with sporadic medullary thyroid carcinoma
O Gimm, H Dziema, J Brown, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 80) with videos related to
Sort By:
Page
of 8
Genes, Chromosomes & Cancer
|
March 1, 1993
Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2
L M Mulligan, E Gardner, B A Smith, et al.
Oncogene
|
May 15, 1998
Analysis of PTEN and the 10q23 region in primary prostate carcinomas
H E Feilotter, M A Nagai, A H Boag, et al.
Human Molecular Genetics
|
March 1, 1993
Localisation of the gene for multiple endocrine neoplasia type 2A to a 480 kb region in chromosome band 10q11.2
S E Mole, L M Mulligan, C S Healey, et al.
Oncogene
|
September 1, 1993
Structural analysis of the human ret proto-oncogene using exon trapping
J B Kwok, E Gardner, J P Warner, et al.
American Journal of Medical Genetics
|
January 1, 1986
An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis
C J Forster-Gibson, L M Mulligan, N E Simpson, et al.
Clinical Genetics
|
February 1, 1997
Mutation of RET codon 768 is associated with the FMTC phenotype
L M Boccia, J S Green, C Joyce, et al.
Cancer Research
|
January 15, 1997
Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas
P L Dahia, S P Toledo, L M Mulligan, et al.
Journal of Medical Genetics
|
September 9, 2000
Characterisation of the human GFRalpha-3 locus and investigation of the gene in Hirschsprung disease
C I Onochie, L M Korngut, J B Vanhorne, et al.
Surgery
|
December 1, 1994
Clinical value of direct DNA analysis of the RET proto-oncogene in families with multiple endocrine neoplasia type 2A
G L Feldman, M Kambouris, G B Talpos, et al.
Oncogene
|
May 22, 2001
Over-representation of a germline variant in the gene encoding RET co-receptor GFRalpha-1 but not GFRalpha-2 or GFRalpha-3 in cases with sporadic medullary thyroid carcinoma
O Gimm, H Dziema, J Brown, et al.
Page
of 8