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US Newborn Screening System Guidelines II: Follow-up of Children, Diagnosis, Management, and Evaluation Statement of the Council of Regional Networks for Genetic Services (CORN)

The Journal of pediatrics, 2000-10, Vol.137 (4), p.S1-S47

2000

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Federal regulations and the future of research in human and medical genetics

The Journal of continuing education in the health professions, 2001, Vol.21 (4), p.238-246

Pelias, Mary Z.

2001

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The USH1C 216G-->A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population

Human genetics, 2002-01, Vol.110 (1), p.95-97

2002

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Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene

Biochimica et biophysica acta, 1998-07, Vol.1407 (1), p.84-91

1998

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Decreased content of docosahexaenoate and arachidonate in plasma phospholipids in usher's syndrome

Biochemical and biophysical research communications, 1986-12, Vol.141 (2), p.600-604

1986

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Medicolegal Aspects of Prenatal Diagnosis

Genetic Disorders and the Fetus, 2011, p.1053-1080

2011

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Localization of two genes for usher syndrome type I to chromosome 11

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.995-1002

1992

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Duty to re-contact

Genetics in medicine, 1999-05, Vol.1 (4), p.171-172

1999

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Recent Developments in Human Behavioral Genetics: Past Accomplishments and Future Directions

American journal of human genetics, 1997, Vol.60 (6), p.1265-1275

1997

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Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11

American journal of human genetics, 1994-04, Vol.54 (4), p.681-686

1994

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Response to Allegations against James V. Neel in Darkness in El Dorado, by Patrick Tierney

American journal of human genetics, 2002-01, Vol.70 (1), p.1-10

2002

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The USHIC 216G→A mutation and the 9-repeat VNTR(t, t) allele are in complete linkage disequilibrium in the Acadian population

Human genetics, 2002, Vol.110 (1), p.95-97

2002

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The Human Genome Project and public perception: truth and consequences

Emory law journal, 2000, Vol.49 (3), p.837-858

2000

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A sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome

American journal of medical genetics, 1981, Vol.10 (2), p.133-139

1981

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Linkage studies of usher syndrome type 1: Exclusion results from the usher syndrome consortium

Genomics (San Diego, Calif.), 1992-11, Vol.14 (3), p.707-714

1992

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Clinical variability and genetic heterogeneity within the Acadian Usher population

American journal of medical genetics, 1992-08, Vol.43 (6), p.964-969

1992

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Duty to disclose: Response to Dr. Borgaonkar

American journal of medical genetics, 1992-12, Vol.44 (6), p.852-853

Pelias, Mary Z.

1992

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Duty to disclose in medical genetics: A legal perspective

American journal of medical genetics, 1991-06, Vol.39 (3), p.347-354

Pelias, Mary Z.

1991

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The duty to disclose to relatives in medical genetics: Response to Dr. Hecht

American journal of medical genetics, 1992-03, Vol.42 (5), p.759-760

Pelias, Mary Z.

1992

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Genetic studies in multiple myeloma 1. Association with HLA‐Cw5

Cancer, 1983-04, Vol.51 (8), p.1408-1411

1983

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Torts of wrongful birth and wrongful life: A review

American journal of medical genetics, 1986-09, Vol.25 (1), p.71-80

1986

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Code of ethical principles for genetics professionals: An explication

American journal of medical genetics, 1996-10, Vol.65 (3), p.179-183

1996

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Code of ethical principles for genetics professionals

American journal of medical genetics, 1996-10, Vol.65 (3), p.177-178

1996

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Baller-Gerold syndrome: An 11th case of craniosynostosis and radial aplasia

American journal of medical genetics, 1990-12, Vol.37 (4), p.447-450

1990

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Maroteaux-Lamy syndrome in a large consanguineous kindred: Biochemical and immunological studies

American journal of medical genetics, 1986-10, Vol.25 (2), p.273-279

1986

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US Newborn Screening System Guidelines II: Follow-up of Children, Diagnosis, Management, and Evaluation Statement of the Council of Regional Networks for Genetic Services (CORN)

Federal regulations and the future of research in human and medical genetics

The USH1C 216G-->A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population

Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene

Decreased content of docosahexaenoate and arachidonate in plasma phospholipids in usher's syndrome

Medicolegal Aspects of Prenatal Diagnosis

Localization of two genes for usher syndrome type I to chromosome 11

Duty to re-contact

Recent Developments in Human Behavioral Genetics: Past Accomplishments and Future Directions

Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11

Response to Allegations against James V. Neel in Darkness in El Dorado, by Patrick Tierney

The USHIC 216G→A mutation and the 9-repeat VNTR(t, t) allele are in complete linkage disequilibrium in the Acadian population

The Human Genome Project and public perception: truth and consequences

A sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome

Linkage studies of usher syndrome type 1: Exclusion results from the usher syndrome consortium

Clinical variability and genetic heterogeneity within the Acadian Usher population

Duty to disclose: Response to Dr. Borgaonkar

Duty to disclose in medical genetics: A legal perspective

The duty to disclose to relatives in medical genetics: Response to Dr. Hecht

Genetic studies in multiple myeloma 1. Association with HLA‐Cw5

Torts of wrongful birth and wrongful life: A review

Code of ethical principles for genetics professionals: An explication

Code of ethical principles for genetics professionals

Baller-Gerold syndrome: An 11th case of craniosynostosis and radial aplasia

Maroteaux-Lamy syndrome in a large consanguineous kindred: Biochemical and immunological studies

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