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Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer

Clinical genetics, 1999-06, Vol.55 (6), p.419-430

1999

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Measuring Women's Preferences for Breast Cancer Treatments and BRCA1/BRCA2 Testing

Quality of life research, 2001-01, Vol.10 (7), p.595-607

2001

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Diagnostic single strand conformational polymorphism, (SSCP) : a simplified non-radioisotopic method as applied to a tay-sachs B1 variant

Nucleic acids research, 1991-01, Vol.19 (2), p.405-406

1991

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Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis

Journal of medical genetics, 1996-12, Vol.33 (12), p.1011-1014

1996

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Some caveats in PCR-based prenatal diagnosis on direct amniotic fluid versus cultured amniocytes

Prenatal diagnosis, 1999-02, Vol.19 (2), p.113-117

1999

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Polyglutamine-containing proteins in schizophrenia: an effect of lymphoblastoid cells?

Molecular psychiatry, 2000-05, Vol.5 (3), p.234-236

2000

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Characterization and Polymerase Chain Reaction (PCR) Detection of an Alu Deletion Polymorphism in Total Linkage Disequilibrium with Myotonic Dystrophy

Genomics (San Diego, Calif.), 1993-02, Vol.15 (2), p.446-448

1993

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The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

Cell, 1995-01, Vol.80 (1), p.167-178

1995

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Correlation between decreased myocardial glucose phosphorylation and DNA mutation size in myotonic dystrophy

Circulation (New York, N.Y.), 1997-03, Vol.95 (6), p.1664-1665

1997

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A Multicopy Dinucleotide Marker That Maps Close to the Spinal Muscular Atrophy Gene

Genomics (San Diego, Calif.), 1994-05, Vol.21 (2), p.394-402

1994

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Molecular characterization of the murine argininosuccinate synthetase locus

Gene, 1991-03, Vol.99 (2), p.181-189

1991

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Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7

Neurogenetics, 1997-11, Vol.1 (2), p.141-147

1997

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Nucleotide sequence of the cDNA encoding the rat argininosuccinate synthetase

Nucleic acids research, 1988-10, Vol.16 (19), p.9352-9352

1988

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Analysis of Trinucleotide Repeats in Myotonic Dystrophy

Current Protocols in Human Genetics, 2001-05, Vol.1 (1), p.9.6.1-9.6.13

2001

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Psychological and social predictors of decisions about genetic testing for breast cancer in high-risk women

Psychology, health & medicine, 2001-08, Vol.6 (3), p.321-333

2001

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Genetic heterogeneity in spinal muscular atrophy: a linkage analysis-based assessment

Neurology, 1994-05, Vol.44 (5), p.919-919

1994

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Physician knowledge and attitudes towards molecular genetic (DNA) testing of their patients

Clinical genetics, 1998-06, Vol.53 (6), p.447-455

1998

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Canadian women's attitudes towards breast cancer gene testing

American journal of human genetics, 1997-10, Vol.61 (4), p.A187-A187

1997

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The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy

Journal of medical genetics, 1992-11, Vol.29 (11), p.774-779

1992

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Deletion and Uniparental Disomy Involving the Same Maternal Chromosome 15

The New England journal of medicine, 1994-02, Vol.330 (8), p.572-573

1994

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Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene

Nature genetics, 1993-07, Vol.4 (3), p.233-238

1993

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Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization

European journal of human genetics : EJHG, 1995, Vol.3 (3), p.195-202

1995

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Simple, rapid detection of PCR heteroduplexes in DNA mutations and polymorphisms

Clinical chemistry (Baltimore, Md.), 1991-12, Vol.37 (12), p.2142-2142

1991

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Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1]

American journal of medical genetics, 1991-10, Vol.41 (1), p.15-17

1991

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A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119)

Nucleic acids research, 1991-03, Vol.19 (5), p.1157-1157

1991

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Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer

Measuring Women's Preferences for Breast Cancer Treatments and BRCA1/BRCA2 Testing

Diagnostic single strand conformational polymorphism, (SSCP) : a simplified non-radioisotopic method as applied to a tay-sachs B1 variant

Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis

Some caveats in PCR-based prenatal diagnosis on direct amniotic fluid versus cultured amniocytes

Polyglutamine-containing proteins in schizophrenia: an effect of lymphoblastoid cells?

Characterization and Polymerase Chain Reaction (PCR) Detection of an Alu Deletion Polymorphism in Total Linkage Disequilibrium with Myotonic Dystrophy

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

Correlation between decreased myocardial glucose phosphorylation and DNA mutation size in myotonic dystrophy

A Multicopy Dinucleotide Marker That Maps Close to the Spinal Muscular Atrophy Gene

Molecular characterization of the murine argininosuccinate synthetase locus

Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7

Nucleotide sequence of the cDNA encoding the rat argininosuccinate synthetase

Analysis of Trinucleotide Repeats in Myotonic Dystrophy

Psychological and social predictors of decisions about genetic testing for breast cancer in high-risk women

Genetic heterogeneity in spinal muscular atrophy: a linkage analysis-based assessment

Physician knowledge and attitudes towards molecular genetic (DNA) testing of their patients

Canadian women's attitudes towards breast cancer gene testing

The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy

Deletion and Uniparental Disomy Involving the Same Maternal Chromosome 15

Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene

Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization

Simple, rapid detection of PCR heteroduplexes in DNA mutations and polymorphisms

Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1]

A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119)

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