Plon SE - Search Results

1

Incidental copy-number variants identified by routine genome testing in a clinical population.

Boone PM, Soens ZT, Campbell IM, Stankiewicz P, Cheung SW, Patel A, Beaudet AL, Plon SE, Shaw CA, McGuire AL, Lupski JR. Boone PM, et al. Among authors: plon se. Genet Med. 2013 Jan;15(1):45-54. doi: 10.1038/gim.2012.95. Epub 2012 Aug 9. Genet Med. 2013. PMID: 22878507 Free PMC article.

2

Psychological impact of receiving negative BRCA1 mutation test results in Ashkenazim.

Friedman LC, Webb JA, Richards CS, Lynch GR, Kaplan AL, Brunicardi FC, Plon SE. Friedman LC, et al. Among authors: plon se. Genet Med. 1999 Mar-Apr;1(3):74-9. doi: 10.1097/00125817-199903000-00003. Genet Med. 1999. PMID: 11336456 Free article.

3

Mammography behavior after receiving a negative BRCA1 mutation test result in the Ashkenazim: a community-based study.

Plon SE, Peterson LE, Friedman LC, Richards CS. Plon SE, et al. Genet Med. 2000 Nov-Dec;2(6):307-11. doi: 10.1097/00125817-200011000-00001. Genet Med. 2000. PMID: 11339650 Free article.

4

FBN1 exon 2 splicing error in a patient with Marfan syndrome.

Guo D, Tan FK, Cantu A, Plon SE, Milewicz DM. Guo D, et al. Among authors: plon se. Am J Med Genet. 2001 Jun 15;101(2):130-4. doi: 10.1002/1096-8628(20010615)101:2<130::aid-ajmg1333>3.0.co;2-v. Am J Med Genet. 2001. PMID: 11391655

5

Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients.

Wang LL, Levy ML, Lewis RA, Chintagumpala MM, Lev D, Rogers M, Plon SE. Wang LL, et al. Among authors: plon se. Am J Med Genet. 2001 Jul 22;102(1):11-7. doi: 10.1002/1096-8628(20010722)102:1<11::aid-ajmg1413>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11471165

6

Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.

Shinawi M, Erez A, Shardy DL, Lee B, Naeem R, Weissenberger G, Chinault AC, Cheung SW, Plon SE. Shinawi M, et al. Among authors: plon se. Blood. 2008 Aug 15;112(4):1042-7. doi: 10.1182/blood-2008-01-135970. Epub 2008 May 16. Blood. 2008. PMID: 18487507 Free PMC article.

7

Phenotypic manifestations of copy number variation in chromosome 16p13.11.

Nagamani SC, Erez A, Bader P, Lalani SR, Scott DA, Scaglia F, Plon SE, Tsai CH, Reimschisel T, Roeder E, Malphrus AD, Eng PA, Hixson PM, Kang SH, Stankiewicz P, Patel A, Cheung SW. Nagamani SC, et al. Among authors: plon se. Eur J Hum Genet. 2011 Mar;19(3):280-6. doi: 10.1038/ejhg.2010.184. Epub 2010 Dec 8. Eur J Hum Genet. 2011. PMID: 21150890 Free PMC article.

8

Genetic testing and cancer risk management recommendations by physicians for at-risk relatives.

Plon SE, Cooper HP, Parks B, Dhar SU, Kelly PA, Weinberg AD, Staggs S, Wang T, Hilsenbeck S. Plon SE, et al. Genet Med. 2011 Feb;13(2):148-54. doi: 10.1097/GIM.0b013e318207f564. Genet Med. 2011. PMID: 21224735 Free PMC article.

9

Unifying cancer genetics.

Plon SE. Plon SE. Genet Med. 2011 Mar;13(3):203-4. doi: 10.1097/GIM.0b013e31820d5e87. Genet Med. 2011. PMID: 21311342 Free PMC article. No abstract available.

10

Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel.

Plon SE, Wheeler DA, Strong LC, Tomlinson GE, Pirics M, Meng Q, Cheung HC, Begin PR, Muzny DM, Lewis L, Biegel JA, Gibbs RA. Plon SE, et al. Cancer Genet. 2011 Jan;204(1):19-25. doi: 10.1016/j.cancergencyto.2010.11.001. Cancer Genet. 2011. PMID: 21356188 Free PMC article.

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