W W Noll - JoVE Visualize

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American Journal of Medical Genetics|July 23, 1998

Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2)J P Park, J B Moeschler, V H Hani, et al.

Clinical Chemistry|March 1, 1997

Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinomaM Siegelman, A Mohabeer, T J Fahey, et al.

Archives of Pathology & Laboratory Medicine|May 13, 1999

Recommended policies for uses of human tissue in research, education, and quality control. Ad Hoc Committee on Stored Tissue, College of American PathologistsW Grizzle, W W Grody, W W Noll, et al.

Cancer|March 1, 1980

Isolation and growth characteristics of continuous cell lines from small-cell carcinoma of the lungO S Pettengill, G D Sorenson, D H Wurster-Hill, et al.

Cancer Genetics and Cytogenetics|November 7, 2000

Amplification of the MLL region in acute myeloid leukemiaJ P Park, S L Ladd, P Ely, et al.

The American Journal of Pathology|February 13, 2001

Loss of heterozygosity on chromosome 11q22-23 in melanoma is associated with retention of the insertion polymorphism in the matrix metalloproteinase-1 promoterW W Noll, D R Belloni, J L Rutter, et al.

Gene|December 22, 1993

Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR productsD T Moir, T E Dorman, F Xue, et al.

Human Molecular Genetics|April 1, 1994

Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic testsF Xue, H Yu, L H Maurer, et al.

American Journal of Medical Genetics|March 2, 1999

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delayT K Mohandas, J P Park, R A Spellman, et al.

Journal of Internal Medicine|October 1, 1995

Genotype-phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation ConsortiumL M Mulligan, D J Marsh, B G Robinson, et al.

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Showing results (11-20 of 22) with videos related to

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Pageof 3

American Journal of Medical Genetics|July 23, 1998

Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2)J P Park, J B Moeschler, V H Hani, et al.

Clinical Chemistry|March 1, 1997

Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinomaM Siegelman, A Mohabeer, T J Fahey, et al.

Archives of Pathology & Laboratory Medicine|May 13, 1999

Recommended policies for uses of human tissue in research, education, and quality control. Ad Hoc Committee on Stored Tissue, College of American PathologistsW Grizzle, W W Grody, W W Noll, et al.

Cancer|March 1, 1980

Isolation and growth characteristics of continuous cell lines from small-cell carcinoma of the lungO S Pettengill, G D Sorenson, D H Wurster-Hill, et al.

Cancer Genetics and Cytogenetics|November 7, 2000

Amplification of the MLL region in acute myeloid leukemiaJ P Park, S L Ladd, P Ely, et al.

The American Journal of Pathology|February 13, 2001

Loss of heterozygosity on chromosome 11q22-23 in melanoma is associated with retention of the insertion polymorphism in the matrix metalloproteinase-1 promoterW W Noll, D R Belloni, J L Rutter, et al.

Gene|December 22, 1993

Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR productsD T Moir, T E Dorman, F Xue, et al.

Human Molecular Genetics|April 1, 1994

Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic testsF Xue, H Yu, L H Maurer, et al.

American Journal of Medical Genetics|March 2, 1999

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delayT K Mohandas, J P Park, R A Spellman, et al.

Journal of Internal Medicine|October 1, 1995

Genotype-phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation ConsortiumL M Mulligan, D J Marsh, B G Robinson, et al.

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