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Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel

Genetics in medicine, 2004-09, Vol.6 (5), p.387-391

2004

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Toward clinical genomics in everyday medicine: perspectives and recommendations

Expert review of molecular diagnostics, 2016-05, Vol.16 (5), p.521-532

2016

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Length of uninterrupted CGG repeats determines instability in the FMR1 gene

Nature genetics, 1994-09, Vol.8 (1), p.88-94

1994

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Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics

Genetics in medicine, 2001-05, Vol.3 (3), p.200-205

2001

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Standards and Guidelines for CFTR Mutation Testing

Genetics in medicine, 2002-09, Vol.4 (5), p.379-391

2002

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Effects of resistance exercise and creatine supplementation on myasthenia gravis : a case study

Medicine and science in sports and exercise, 2001-06, Vol.33 (6), p.869-872

2001

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Technical standards and guidelines: Venous thromboembolism (Factor V Leiden and prothrombin 20210G>A testing): A disease-specific supplement to the standards and guidelines for clinical genetics laboratories

Genetics in medicine, 2005-07, Vol.7 (6), p.444-453

2005

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Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes

American journal of clinical pathology, 2001-03, Vol.115 (3), p.439-447

2001

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Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation

Human molecular genetics, 1999-11, Vol.8 (12), p.2293-2302

1999

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Protein requirements for optimal nitrogen retention in resistance-trained individuals

Proceedings of the West Virginia Academy of Science, 2017-04, Vol.89 (1)

2017

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Cystic fibrosis carrier screening: Issues in implementation

Genetics in medicine, 2002-11, Vol.4 (6), p.407-409

2002

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Advances for proficiency testing for genetic laboratory science

Accreditation and quality assurance, 2002-09, Vol.7 (8-9), p.351-356

POPOVICH, Bradley W

2002

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Spinal strength and range of motion in adults with scoliosis

Proceedings of the West Virginia Academy of Science, 2017-04, Vol.89 (1)

2017

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A novel CAG repeat configuration in the SCA1 gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1

Human molecular genetics, 1995-12, Vol.4 (12), p.2411-2413

1995

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Augmented protein intake for athletes: Are safety concerns well founded?

Journal of chiropractic medicine, 2003-01, Vol.2 (1), p.13-15

2003

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A Small 55-Repeat MJD1 CAG Allele in a Patient with Machado-Joseph Disease and Abnormal Eye Movements

European neurology, 2000-01, Vol.44 (3), p.189-190

2000

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Naming and counting disorders (conditions) included in newborn screening panels

Pediatrics (Evanston), 2006-05, Vol.117 (5 Pt 2), p.S308

2006

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Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy

American journal of human genetics, 1997, Vol.60 (1), p.160-165

1997

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GeneTests-GeneClinics: Genetic testing information for a growing audience

Human mutation, 2002-05, Vol.19 (5), p.501-509

2002

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Therapeutic Modalities for Athletic Injuries

Journal of Chiropractic Medicine, 2003-01, Vol.2 (1), p.41-41

Bradley-Popovich, Greg

2003

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Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism

Human molecular genetics, 1995-09, Vol.4 (9), p.1681-1684

1995

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Hypomethylation of an Expanded FMR1 Allele Is Not Associated with a Global DNA Methylation Defect

American journal of human genetics, 1999-11, Vol.65 (5), p.1375-1386

1999

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An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene

American journal of human genetics, 1995-05, Vol.56 (5), p.1042-1051

1995

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Fragile X full mutations are more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics

Genetics in medicine, 2000-07, Vol.2 (4), p.242-248

2000

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A small 55-repeat MJDL CAG allele in a patient with Machado-Joseph disease and abnormal eye movements

European neurology, 2000, Vol.44 (3), p.189-190

2000

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Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel

Toward clinical genomics in everyday medicine: perspectives and recommendations

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics

Standards and Guidelines for CFTR Mutation Testing

Effects of resistance exercise and creatine supplementation on myasthenia gravis : a case study

Technical standards and guidelines: Venous thromboembolism (Factor V Leiden and prothrombin 20210G>A testing): A disease-specific supplement to the standards and guidelines for clinical genetics laboratories

Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes

Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation

Protein requirements for optimal nitrogen retention in resistance-trained individuals

Cystic fibrosis carrier screening: Issues in implementation

Advances for proficiency testing for genetic laboratory science

Spinal strength and range of motion in adults with scoliosis

A novel CAG repeat configuration in the SCA1 gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1

Augmented protein intake for athletes: Are safety concerns well founded?

A Small 55-Repeat MJD1 CAG Allele in a Patient with Machado-Joseph Disease and Abnormal Eye Movements

Naming and counting disorders (conditions) included in newborn screening panels

Uniparental disomy of the entire X chromosome in a female with Duchenne muscular dystrophy

GeneTests-GeneClinics: Genetic testing information for a growing audience

Therapeutic Modalities for Athletic Injuries

Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism

Hypomethylation of an Expanded FMR1 Allele Is Not Associated with a Global DNA Methylation Defect

An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene

Fragile X full mutations are more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics

A small 55-repeat MJDL CAG allele in a patient with Machado-Joseph disease and abnormal eye movements

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