1. The Role of MMAC1 Mutations in Early-Onset Breast Cancer: Causative in Association with Cowden Syndrome and Excluded in BRCA1-Negative Cases 
Hui C. Tsou, David H.-F. Teng, Xiao Li Ping, Valeria Brancolini, Thaylon Davis, Rong Hu, Xiao Xun Xie, Alexandra C. Gruener, Carolina A. Schrager, Angela M. Christiano, Charis Eng, Peter Steck, Jurg Ott, Sean V. Tavtigian, Monica Peacocke 
The American Journal of Human Genetics 
Volume 61, Issue 5, Pages (November 1997)
DOI: /301607
Copyright © 1997 The American Society of Human Genetics Terms and Conditions

2. Figure 1
Haplotype construction with markers on chromosome 10 in four families with CS
The American Journal of Human Genetics  , DOI: ( /301607)
Copyright © 1997 The American Society of Human Genetics Terms and Conditions

3. Figure 2
DNA Sequencing of MMAC1 in a family with CS and early-onset breast cancer. The affected mother (blackened circle) demonstrates a 2-bp insertion (AT) in exon 5, which is not seen in her unaffected brother (unblackened square). Her affected daughter has inherited the AT insertion.
The American Journal of Human Genetics  , DOI: ( /301607)
Copyright © 1997 The American Society of Human Genetics Terms and Conditions