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BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer

Cancer, 2009-05, Vol.115 (10), p.2222-2233

2009

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The relationship of APOE genotype to neuropsychological performance in long-term cancer survivors treated with standard dose chemotherapy

Psycho-oncology (Chichester, England), 2003-09, Vol.12 (6), p.612-619

2003

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Randomized clinical trial of PCR–determined human papillomavirus detection methods: Self-sampling versus clinician-directed–Biologic concordance and women's preferences

American journal of obstetrics and gynecology, 2002-03, Vol.186 (3), p.365-373

2002

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Recommended Policies for Uses of Human Tissue in Research, Education, and Quality Control

Archives of pathology & laboratory medicine (1976), 1999-04, Vol.123 (4), p.296-300

1999

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Factors affecting the detection rate of human papillomavirus

Annals of family medicine, 2003-11, Vol.1 (4), p.221-227

2003

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Loss of Heterozygosity on Chromosome 11q22-23 in Melanoma Is Associated with Retention of the Insertion Polymorphism in the Matrix Metalloproteinase-1 Promoter

The American journal of pathology, 2001-02, Vol.158 (2), p.691-697

2001

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Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma

Clinical endocrinology (Oxford), 2005-12, Vol.63 (6), p.676-682

2005

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A Novel Method for Creating Artificial Mutant Samples for Performance Evaluation and Quality Control in Clinical Molecular Genetics

The Journal of molecular diagnostics : JMD, 2005-05, Vol.7 (2), p.247-251

2005

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Tampon Samplings With Longer Cervicovaginal Cell Exposures Are Equivalent to Two Consecutive Swabs for the Detection of High-Risk Human Papillomavirus

Sexually transmitted diseases, 2002-11, Vol.29 (11), p.628-636

2002

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Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results

Nature genetics, 1999-11, Vol.23 (3), p.271-272

1999

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Utility of RET mutation analysis in multiple endocrine neoplasia type 2

Archives of pathology & laboratory medicine (1976), 1999-11, Vol.123 (11), p.1047-1049

Noll, W W

1999

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Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion

Human pathology, 1999-05, Vol.30 (5), p.577-581

1999

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Multicenter evaluation of PCR methods for the detection of factor V Leiden (R506Q) genotypes

Clinical chemistry (Baltimore, Md.), 1998-06, Vol.44 (6), p.1356-1358

1998

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Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma

Clinical chemistry (Baltimore, Md.), 1997-03, Vol.43 (3), p.453-457

1997

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Amplification of the MLL Region in Acute Myeloid Leukemia

Cancer genetics and cytogenetics, 2000-09, Vol.121 (2), p.198-205

2000

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Chemistry and Technology of Silicones

Noll, Walter

1, 1968

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A cytogenetic study of familial medullary carcinoma of the thyroid

Cancer research (Chicago, Ill.), 1986-04, Vol.46 (4), p.2134-2138

1986

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Diversity of Cystic Fibrosis Mutation-Screening Practices

American journal of human genetics, 1998-05, Vol.62 (5), p.1252-1254

1998

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Identification of a second human acetyl-CoA carboxylase gene

Biochemical journal, 1996-06, Vol.316 ( Pt 3) (3), p.915-922

1996

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Estimate of prevalence of proximal 15q duplication syndrome

American journal of medical genetics, 2002-09, Vol.111 (4), p.440-442

2002

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Causes of dark urine

JAMA : the journal of the American Medical Association, 1980-06, Vol.243 (23), p.2398

1980

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Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests

Human molecular genetics, 1994-04, Vol.3 (4), p.635-638

1994

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Detection of Human DNA Polymorphisms with a Simplified Denaturing Gradient Gel Electrophoresis Technique

Proceedings of the National Academy of Sciences - PNAS, 1987-05, Vol.84 (10), p.3339-3343

1987

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NOVEL 2905-BP MITOCHONDRIAL DNA DELETION IN KEARNS-SAYRE SYNDROME: 170

Journal of neuropathology and experimental neurology, 1995-05, Vol.54 (3), p.453

1995

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Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products

Gene, 1993-12, Vol.136 (1), p.177-183

1993

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BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer

The relationship of APOE genotype to neuropsychological performance in long-term cancer survivors treated with standard dose chemotherapy

Randomized clinical trial of PCR–determined human papillomavirus detection methods: Self-sampling versus clinician-directed–Biologic concordance and women's preferences

Recommended Policies for Uses of Human Tissue in Research, Education, and Quality Control

Factors affecting the detection rate of human papillomavirus

Loss of Heterozygosity on Chromosome 11q22-23 in Melanoma Is Associated with Retention of the Insertion Polymorphism in the Matrix Metalloproteinase-1 Promoter

Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma

A Novel Method for Creating Artificial Mutant Samples for Performance Evaluation and Quality Control in Clinical Molecular Genetics

Tampon Samplings With Longer Cervicovaginal Cell Exposures Are Equivalent to Two Consecutive Swabs for the Detection of High-Risk Human Papillomavirus

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results

Utility of RET mutation analysis in multiple endocrine neoplasia type 2

Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion

Multicenter evaluation of PCR methods for the detection of factor V Leiden (R506Q) genotypes

Rapid, nonradioactive screening for mutations in exons 10, 11, and 16 of the RET protooncogene associated with inherited medullary thyroid carcinoma

Amplification of the MLL Region in Acute Myeloid Leukemia

Chemistry and Technology of Silicones

A cytogenetic study of familial medullary carcinoma of the thyroid

Diversity of Cystic Fibrosis Mutation-Screening Practices

Identification of a second human acetyl-CoA carboxylase gene

Estimate of prevalence of proximal 15q duplication syndrome

Causes of dark urine

Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests

Detection of Human DNA Polymorphisms with a Simplified Denaturing Gradient Gel Electrophoresis Technique

NOVEL 2905-BP MITOCHONDRIAL DNA DELETION IN KEARNS-SAYRE SYNDROME: 170

Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products

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