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L M Mulligan

Showing results (41-50 of 80) with videos related to

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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 systemS 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 neurofibromatosisW 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 tumorsM 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 splicingM 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 diseaseT Attie, A Pelet, P Sarda, et al.
Cancer Research|May 1, 1996
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinomaC 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 familiesD 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 locusP Edery, A Pelet, L M Mulligan, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 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 systemS 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 neurofibromatosisW 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 tumorsM 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 splicingM 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 diseaseT Attie, A Pelet, P Sarda, et al.
Cancer Research|May 1, 1996
Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinomaC 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 familiesD 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 locusP Edery, A Pelet, L M Mulligan, et al.
Pageof 8