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Journal of Medical Genetics
|
April 1, 1994
Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?
M S Fewtrell, P K Tam, A H Thomson, et al.
Nucleic Acids Research
|
July 11, 1986
A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h]
K Wrogemann, B Arveiler, I Oberle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 20, 2001
Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system
S Gläsker, B U Bender, T W Apel, et al.
Genes, Chromosomes & Cancer
|
June 1, 1992
Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis
W Xu, L M Mulligan, M A Ponder, et al.
Oncology
|
November 1, 1995
Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors
M A Nagai, A C Medeiros, M M Brentani, et al.
Oncogene
|
April 6, 1995
Multiple mRNA isoforms of the human RET proto-oncogene generated by alternate splicing
M J Lorenzo, C Eng, L M Mulligan, et al.
Human Molecular Genetics
|
August 1, 1994
A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung's disease
T Attie, A Pelet, P Sarda, et al.
Cancer Research
|
May 1, 1996
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma
C Eng, L M Mulligan, C S Healey, et al.
Genomics
|
September 15, 1994
A rapid screening method for the detection of mutations in the RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families
D J Marsh, B G Robinson, S Andrew, et al.
Journal of Medical Genetics
|
August 1, 1994
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus
P Edery, A Pelet, L M Mulligan, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 80) with videos related to
Sort By:
Page
of 8
Journal of Medical Genetics
|
April 1, 1994
Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?
M S Fewtrell, P K Tam, A H Thomson, et al.
Nucleic Acids Research
|
July 11, 1986
A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h]
K Wrogemann, B Arveiler, I Oberle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 20, 2001
Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system
S Gläsker, B U Bender, T W Apel, et al.
Genes, Chromosomes & Cancer
|
June 1, 1992
Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis
W Xu, L M Mulligan, M A Ponder, et al.
Oncology
|
November 1, 1995
Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors
M A Nagai, A C Medeiros, M M Brentani, et al.
Oncogene
|
April 6, 1995
Multiple mRNA isoforms of the human RET proto-oncogene generated by alternate splicing
M J Lorenzo, C Eng, L M Mulligan, et al.
Human Molecular Genetics
|
August 1, 1994
A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung's disease
T Attie, A Pelet, P Sarda, et al.
Cancer Research
|
May 1, 1996
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma
C Eng, L M Mulligan, C S Healey, et al.
Genomics
|
September 15, 1994
A rapid screening method for the detection of mutations in the RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families
D J Marsh, B G Robinson, S Andrew, et al.
Journal of Medical Genetics
|
August 1, 1994
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus
P Edery, A Pelet, L M Mulligan, et al.
Page
of 8