Volume 3 Issue 2, March 2001

Down syndrome congenital heart disease: A narrowed region and a candidate gene

• Gillian M Barlow
• Xiao-Ning Chen
• Julie R Korenberg

A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: Fluorescence in situ hybridization and dosage-sensitive Southern blot analysis

• Karen W Gripp
• Viera Kasparcova
• Catherine A Stolle

Hemochromatosis-associated morbidity in the United States: An analysis of the National Hospital Discharge Survey, 1979–1997

• Amanda S Brown
• Marta Gwinn
• Muin J Khoury

Genetic testing for breast cancer: Where are health care providers in the decision process?

• Christine M Velicer
• Stephen Taplin

Oncologists' opinions on genetic testing for breast and ovarian cancer

• Julie O Culver
• Judy L Hull
• Wylie Burke

Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel

• Cathy M Tuck-Muller
• Barbara K Goodman
• Gail Stetten

Recombinant human acid α-glucosidase enzyme therapy for infantile glycogen storage disease type II: Results of a phase I/II clinical trial

• Andrea Amalfitano
• A. Resai Bengur
• Yuan-Tsong Chen

American College of Medical Genetics Consensus Statement on Factor V Leiden Mutation Testing

• Wayne W Grody
• John H Griffin
• John A Heit

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

• Wayne W Grody
• Garry R Cutting
• Robert J Desnick

Recommendations of core competencies in genetics essential for all health professionals

• Jean Jenkins
• Miriam Blitzer
• Alan E Guttmacher

Reviewer Acknowledgment

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