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Clinical Chemistry|February 13, 2001
Capillary and microchip electrophoresis for rapid detection of known mutations by combining allele-specific DNA amplification with heteroduplex analysisH Tian, L C Brody, S Fan, et al.
The Journal of Biological Chemistry|August 1, 1997
Defects in auxiliary redox proteins lead to functional methionine synthase deficiencyS Gulati, Z Chen, L C Brody, et al.
Biochimica Et Biophysica Acta|January 8, 1999
Molecular cloning of the human HAND2 geneM W Russell, P Kemp, L Wang, et al.
JAMA|April 21, 1993
Genetic counseling for families with inherited susceptibility to breast and ovarian cancerB B Biesecker, M Boehnke, K Calzone, et al.
American Journal of Medical Genetics|August 18, 2000
Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian cancer familiesB B Biesecker, N Ishibe, D W Hadley, et al.
Public Health Genomics|September 5, 2009
Considerations for designing a prototype genetic test for use in translational researchC H Wade, C M McBride, S L R Kardia, et al.
Molecular Genetics and Metabolism|March 18, 2000
BRCA1 suppresses insulin-like growth factor-I receptor promoter activity: potential interaction between BRCA1 and Sp1S B Maor, S Abramovitch, M R Erdos, et al.
American Journal of Human Genetics|March 26, 1999
The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi JewsP Hartge, J P Struewing, S Wacholder, et al.
Clinical Genetics|April 15, 2015
Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young ageK A Kaphingst, J Ivanovich, B B Biesecker, et al.
Clinical Genetics|June 15, 2012
Effects of informed consent for individual genome sequencing on relevant knowledgeK A Kaphingst, F M Facio, M-R Cheng, et al.
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