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Archives of Pathology & Laboratory Medicine|October 28, 1999
Utility of RET mutation analysis in multiple endocrine neoplasia type 2W W NollProceedings of the National Academy of Sciences of the United States of America|May 1, 1987
Detection of human DNA polymorphisms with a simplified denaturing gradient gel electrophoresis techniqueW W Noll, M CollinsCancer Genetics and Cytogenetics|February 1, 1996
Constitutional de novo t(1;22)(p22;q11.2) and ependymomaJ P Park, S Chaffee, W W Noll, et al.Human Pathology|May 20, 1999
Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletionM W Becher, M L Wills, W W Noll, et al.Cancer Research|April 1, 1986
A cytogenetic study of familial medullary carcinoma of the thyroidD H Wurster-Hill, W W Noll, L Y Bircher, et al.Cancer Genetics and Cytogenetics|February 15, 1986
Cytogenetics of medullary carcinoma of the thyroidD H Wurster-Hill, W W Noll, L Y Bircher, et al.Cancer Genetics and Cytogenetics|July 15, 1990
Hypodiploid, pseudodiploid, and normal karyotypes prevail in cytogenetic studies of medullary carcinomas of the thyroid and metastatic tissuesD H Wurster-Hill, O S Pettengill, W W Noll, et al.Cancer Genetics and Cytogenetics|October 15, 1988
Fragile sites and high-resolution chromosome studies in multiple endocrine neoplasia type 2AD H Wurster-Hill, W W Noll, J T Devlin, et al.Somatic Cell and Molecular Genetics|January 1, 1994
Localization of acyl coenzyme A:cholesterol acyltransferase gene to human chromosome 1q25C C Chang, W W Noll, N Nutile-McMenemy, et al.Genomics|May 1, 1992
Characterization of radiation/fusion hybrids containing parts of human chromosome 10 and their use in mapping chromosome 10-specific probesC B Rothschild, W W Noll, T C Gravius, et al.Pageof 3