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Heterozygote journal articles from PubMed MEDLINE database

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Lynch HT, Marcus JN, Rubinstein WS 
Stemming the tide of cancer for BRCA1/2 mutation carriers. [Comment, Editorial, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
J Clin Oncol 2008 Sep 10; 26(26):4239-43.
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Alder JK, Chen JJ, Lancaster L, et al. 
Short telomeres are a risk factor for idiopathic pulmonary fibrosis. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Proc Natl Acad Sci U S A 2008 Sep 2; 105(35):13051-6.
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Lavin MF, Kozlov S, Gueven N, et al. 
Atm and cellular response to DNA damage. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Adv Exp Med Biol 2005.:457-76.
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Shaw SW, Cheng PJ, Chang SD, et al. 
Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system. [JOURNAL ARTICLE]
Acta Obstet Gynecol Scand 2008 Aug 11.:1-9.
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Brownlow RJ, Dawson DA, Horsburgh GJ, et al. 
A method for genotype validation and primer assessment in heterozygote-deficient species, as demonstrated in the prosobranch mollusc Hydrobia ulvae. [JOURNAL ARTICLE]
BMC Genet 2008 Aug 19; 9(1):55.
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Tekeli A, Isbir S, Ergen A, et al. 
APE1 and XRCC3 polymorphisms and myocardial infarction. [Journal Article]
In Vivo 2008 Jul-Aug; 22(4):477-9.
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Schover LR 
A lesser evil: prophylactic mastectomy for women at high risk for breast cancer. [Comment, Editorial]
J Clin Oncol 2008 Aug 20; 26(24):3918-9.
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Valle L, Serena-Acedo T, Liyanarachchi S, et al. 
Germline allele-specific expression of TGFBR1 confers an increased risk of colorectal cancer. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Science 2008 Sep 5; 321(5894):1361-5.
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Woon ST, Ameratunga R, Croxson M, et al. 
Follicular lymphoma in a X-linked lymphoproliferative syndrome carrier female. [Journal Article, Research Support, Non-U.S. Gov't]
Scand J Immunol 2008 Aug; 68(2):153-8.
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Al-Thihli K, Rudkin T, Carson N, et al. 
Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Aug 12.
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