D J Marsh|D L Learoyd|B G Robinson - JoVE Visualize

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Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|February 1, 1997

Technetium-99m-sestamibi scanning in recurrent medullary thyroid carcinomaD L Learoyd, P J Roach, G M Briggs, et al.

Biochemical and Biophysical Research Communications|December 14, 1995

Quantitation of APC mRNA in human tissuesM Schnitzler, T Dwight, D J Marsh, et al.

The British Journal of Surgery|April 12, 2001

Expression of the RET proto-oncogene in papillary thyroid carcinoma and its correlation with clinical outcomeP Kjellman, D L Learoyd, M Messina, et al.

Henry Ford Hospital Medical Journal|January 1, 1992

Medullary thyroid carcinoma: Australian experience with genetic testingJ L Ward, V J Hyland, D S Andrew, et al.

Genes, Chromosomes & Cancer|October 27, 1999

Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathwaysJ J Yeh, D J Marsh, J Zedenius, et al.

Thyroid : Official Journal of the American Thyroid Association|January 1, 1992

Postpartum thyroid dysfunctionD L Learoyd, H Y Fung, A M McGregor

Journal of Medical Genetics|March 10, 2001

Male breast cancer in Cowden syndrome patients with germline PTEN mutationsJ D Fackenthal, D J Marsh, A L Richardson, et al.

The Journal of Clinical Endocrinology and Metabolism|August 15, 2001

Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic ricketsI A Holm, A E Nelson, B G Robinson, 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.

Neoplasia (New York, N.Y.)|August 9, 2001

Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatographyD J Marsh, G Theodosopoulos, V Howell, et al.

Pageof 22

Showing results (11-20 of 211) with videos related to

Sort By:

Pageof 22

Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|February 1, 1997

Technetium-99m-sestamibi scanning in recurrent medullary thyroid carcinomaD L Learoyd, P J Roach, G M Briggs, et al.

Biochemical and Biophysical Research Communications|December 14, 1995

Quantitation of APC mRNA in human tissuesM Schnitzler, T Dwight, D J Marsh, et al.

The British Journal of Surgery|April 12, 2001

Expression of the RET proto-oncogene in papillary thyroid carcinoma and its correlation with clinical outcomeP Kjellman, D L Learoyd, M Messina, et al.

Henry Ford Hospital Medical Journal|January 1, 1992

Medullary thyroid carcinoma: Australian experience with genetic testingJ L Ward, V J Hyland, D S Andrew, et al.

Genes, Chromosomes & Cancer|October 27, 1999

Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathwaysJ J Yeh, D J Marsh, J Zedenius, et al.

Thyroid : Official Journal of the American Thyroid Association|January 1, 1992

Postpartum thyroid dysfunctionD L Learoyd, H Y Fung, A M McGregor

Journal of Medical Genetics|March 10, 2001

Male breast cancer in Cowden syndrome patients with germline PTEN mutationsJ D Fackenthal, D J Marsh, A L Richardson, et al.

The Journal of Clinical Endocrinology and Metabolism|August 15, 2001

Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic ricketsI A Holm, A E Nelson, B G Robinson, 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.

Neoplasia (New York, N.Y.)|August 9, 2001

Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatographyD J Marsh, G Theodosopoulos, V Howell, et al.

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