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Items: 1 to 50 of 57

1.

Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting.

Clarke EV, Muessig KR, Zepp J, Hunter JE, Syngal S, Acheson LS, Wiesner GL, Peterson SK, Bergen KM, Shuster E, Davis JV, Schneider JL, Kauffman TL, Gilmore MJ, Reiss JA, Rope AF, Cook JE, Goddard KAB.

Fam Cancer. 2019 Jul;18(3):317-325. doi: 10.1007/s10689-019-00123-x.

PMID:
30729418
2.

Subsequent breast and high grade serous carcinomas after risk-reducing salpingo-oophorectomy in BRCA mutation carriers and patients with history of breast cancer.

Straub MM, Podoll MB, David SN, Wiesner GL, Desouki MM.

Ann Diagn Pathol. 2018 Oct;36:28-30. doi: 10.1016/j.anndiagpath.2018.06.003. Epub 2018 Jun 27.

PMID:
30055521
3.

Physicians' perspectives on receiving unsolicited genomic results.

Pet DB, Holm IA, Williams JL, Myers MF, Novak LL, Brothers KB, Wiesner GL, Clayton EW.

Genet Med. 2019 Feb;21(2):311-318. doi: 10.1038/s41436-018-0047-z. Epub 2018 Jul 5.

4.

The impact of variant classification on the clinical management of hereditary cancer syndromes.

Turner SA, Rao SK, Morgan RH, Vnencak-Jones CL, Wiesner GL.

Genet Med. 2019 Feb;21(2):426-430. doi: 10.1038/s41436-018-0063-z. Epub 2018 Jun 6.

PMID:
29875428
5.

Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews.

Schneider JL, Goddard KAB, Muessig KR, Davis JV, Rope AF, Hunter JE, Peterson SK, Acheson LS, Syngal S, Wiesner GL, Reiss JA.

Hered Cancer Clin Pract. 2018 May 10;16:11. doi: 10.1186/s13053-018-0090-4. eCollection 2018.

6.

Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.

Fossey R, Kochan D, Winkler E, Pacyna JE, Olson J, Thibodeau S, Connolly JJ, Harr M, Behr MA, Prows CA, Cobb B, Myers MF, Leslie ND, Namjou-Khales B, Milo Rasouly H, Wynn J, Fedotov A, Chung WK, Gharavi A, Williams JL, Pais L, Holm I, Aufox S, Smith ME, Scrol A, Leppig K, Jarvik GP, Wiesner GL, Li R, Stroud M, Smoller JW, Sharp RR, Kullo IJ.

J Pers Med. 2018 Jan 3;8(1). pii: E2. doi: 10.3390/jpm8010002.

7.

Identification and Management of TP53 Gene Carriers Detected Through Multigene Panel Testing.

Pal T, Brzosowicz J, Valladares A, Wiesner GL, Laronga C.

South Med J. 2017 Oct;110(10):643-648. doi: 10.14423/SMJ.0000000000000711.

PMID:
28973705
8.

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.

Daly MB, Pilarski R, Berry M, Buys SS, Farmer M, Friedman S, Garber JE, Kauff ND, Khan S, Klein C, Kohlmann W, Kurian A, Litton JK, Madlensky L, Merajver SD, Offit K, Pal T, Reiser G, Shannon KM, Swisher E, Vinayak S, Voian NC, Weitzel JN, Wick MJ, Wiesner GL, Dwyer M, Darlow S.

J Natl Compr Canc Netw. 2017 Jan;15(1):9-20.

PMID:
28040716
9.

Ethical, Legal, and Social Implications of Personalized Genomic Medicine Research: Current Literature and Suggestions for the Future.

Callier SL, Abudu R, Mehlman MJ, Singer ME, Neuhauser D, Caga-Anan C, Wiesner GL.

Bioethics. 2016 Nov;30(9):698-705. doi: 10.1111/bioe.12285. Review.

PMID:
27767224
10.

Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.

Daly MB, Pilarski R, Axilbund JE, Berry M, Buys SS, Crawford B, Farmer M, Friedman S, Garber JE, Khan S, Klein C, Kohlmann W, Kurian A, Litton JK, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Rana H, Reiser G, Robson ME, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wick MJ, Wiesner GL, Dwyer M, Kumar R, Darlow S.

J Natl Compr Canc Netw. 2016 Feb;14(2):153-62.

PMID:
26850485
11.

Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers.

Hunter JE, Zepp JM, Gilmore MJ, Davis JV, Esterberg EJ, Muessig KR, Peterson SK, Syngal S, Acheson LS, Wiesner GL, Reiss JA, Goddard KA.

Cancer. 2015 Sep 15;121(18):3281-9. doi: 10.1002/cncr.29470. Epub 2015 Jun 2.

12.

Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators.

Schneider JL, Davis J, Kauffman TL, Reiss JA, McGinley C, Arnold K, Zepp J, Gilmore M, Muessig KR, Syngal S, Acheson L, Wiesner GL, Peterson SK, Goddard KA.

Genet Med. 2016 Feb;18(2):152-61. doi: 10.1038/gim.2015.43. Epub 2015 Apr 16.

13.

A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.

Hampel H, Bennett RL, Buchanan A, Pearlman R, Wiesner GL; Guideline Development Group, American College of Medical Genetics and Genomics Professional Practice and Guidelines Committee and National Society of Genetic Counselors Practice Guidelines Committee.

Genet Med. 2015 Jan;17(1):70-87. doi: 10.1038/gim.2014.147. Epub 2014 Nov 13.

PMID:
25394175
14.

Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.

Daly MB, Pilarski R, Axilbund JE, Buys SS, Crawford B, Friedman S, Garber JE, Horton C, Kaklamani V, Klein C, Kohlmann W, Kurian A, Litton J, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Pasche B, Reiser G, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wiesner GL, Dwyer MA, Kumar R; National comprehensive cancer network.

J Natl Compr Canc Netw. 2014 Sep;12(9):1326-38.

PMID:
25190698
15.

Inactivating mutation in the prostaglandin transporter gene, SLCO2A1, associated with familial digital clubbing, colon neoplasia, and NSAID resistance.

Guda K, Fink SP, Milne GL, Molyneaux N, Ravi L, Lewis SM, Dannenberg AJ, Montgomery CG, Zhang S, Willis J, Wiesner GL, Markowitz SD.

Cancer Prev Res (Phila). 2014 Aug;7(8):805-12. doi: 10.1158/1940-6207.CAPR-14-0108. Epub 2014 May 16.

16.

Genetics researchers' and IRB professionals' attitudes toward genetic research review: a comparative analysis.

Edwards KL, Lemke AA, Trinidad SB, Lewis SM, Starks H, Snapinn KW, Griffin MQ, Wiesner GL, Burke W; GRRIP Consortium.

Genet Med. 2012 Feb;14(2):236-42. doi: 10.1038/gim.2011.57. Epub 2012 Jan 12.

17.

IRB perspectives on the return of individual results from genomic research.

Dressler LG, Smolek S, Ponsaran R, Markey JM, Starks H, Gerson N, Lewis S, Press N, Juengst E, Wiesner GL; GRRIP Consortium.

Genet Med. 2012 Feb;14(2):215-22. doi: 10.1038/gim.2011.10. Epub 2012 Jan 5.

18.

Attitudes toward genetic research review: results from a survey of human genetics researchers.

Edwards KL, Lemke AA, Trinidad SB, Lewis SM, Starks H, Quinn Griffin MT, Wiesner GL.

Public Health Genomics. 2011;14(6):337-45. doi: 10.1159/000324931. Epub 2011 Apr 11.

19.

Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22.

Gray-McGuire C, Guda K, Adrianto I, Lin CP, Natale L, Potter JD, Newcomb P, Poole EM, Ulrich CM, Lindor N, Goode EL, Fridley BL, Jenkins R, Le Marchand L, Casey G, Haile R, Hopper J, Jenkins M, Young J, Buchanan D, Gallinger S, Adams M, Lewis S, Willis J, Elston R, Markowitz SD, Wiesner GL.

Cancer Res. 2010 Jul 1;70(13):5409-18. doi: 10.1158/0008-5472.CAN-10-0188. Epub 2010 Jun 15.

20.

International network of cancer genome projects.

International Cancer Genome Consortium, Hudson TJ, Anderson W, Artez A, Barker AD, Bell C, Bernabé RR, Bhan MK, Calvo F, Eerola I, Gerhard DS, Guttmacher A, Guyer M, Hemsley FM, Jennings JL, Kerr D, Klatt P, Kolar P, Kusada J, Lane DP, Laplace F, Youyong L, Nettekoven G, Ozenberger B, Peterson J, Rao TS, Remacle J, Schafer AJ, Shibata T, Stratton MR, Vockley JG, Watanabe K, Yang H, Yuen MM, Knoppers BM, Bobrow M, Cambon-Thomsen A, Dressler LG, Dyke SO, Joly Y, Kato K, Kennedy KL, Nicolás P, Parker MJ, Rial-Sebbag E, Romeo-Casabona CM, Shaw KM, Wallace S, Wiesner GL, Zeps N, Lichter P, Biankin AV, Chabannon C, Chin L, Clément B, de Alava E, Degos F, Ferguson ML, Geary P, Hayes DN, Hudson TJ, Johns AL, Kasprzyk A, Nakagawa H, Penny R, Piris MA, Sarin R, Scarpa A, Shibata T, van de Vijver M, Futreal PA, Aburatani H, Bayés M, Botwell DD, Campbell PJ, Estivill X, Gerhard DS, Grimmond SM, Gut I, Hirst M, López-Otín C, Majumder P, Marra M, McPherson JD, Nakagawa H, Ning Z, Puente XS, Ruan Y, Shibata T, Stratton MR, Stunnenberg HG, Swerdlow H, Velculescu VE, Wilson RK, Xue HH, Yang L, Spellman PT, Bader GD, Boutros PC, Campbell PJ, Flicek P, Getz G, Guigó R, Guo G, Haussler D, Heath S, Hubbard TJ, Jiang T, Jones SM, Li Q, López-Bigas N, Luo R, Muthuswamy L, Ouellette BF, Pearson JV, Puente XS, Quesada V, Raphael BJ, Sander C, Shibata T, Speed TP, Stein LD, Stuart JM, Teague JW, Totoki Y, Tsunoda T, Valencia A, Wheeler DA, Wu H, Zhao S, Zhou G, Stein LD, Guigó R, Hubbard TJ, Joly Y, Jones SM, Kasprzyk A, Lathrop M, López-Bigas N, Ouellette BF, Spellman PT, Teague JW, Thomas G, Valencia A, Yoshida T, Kennedy KL, Axton M, Dyke SO, Futreal PA, Gerhard DS, Gunter C, Guyer M, Hudson TJ, McPherson JD, Miller LJ, Ozenberger B, Shaw KM, Kasprzyk A, Stein LD, Zhang J, Haider SA, Wang J, Yung CK, Cros A, Liang Y, Gnaneshan S, Guberman J, Hsu J, Bobrow M, Chalmers DR, Hasel KW, Joly Y, Kaan TS, Kennedy KL, Knoppers BM, Lowrance WW, Masui T, Nicolás P, Rial-Sebbag E, Rodriguez LL, Vergely C, Yoshida T, Grimmond SM, Biankin AV, Bowtell DD, Cloonan N, deFazio A, Eshleman JR, Etemadmoghadam D, Gardiner BB, Kench JG, Scarpa A, Sutherland RL, Tempero MA, Waddell NJ, Wilson PJ, McPherson JD, Gallinger S, Tsao MS, Shaw PA, Petersen GM, Mukhopadhyay D, Chin L, DePinho RA, Thayer S, Muthuswamy L, Shazand K, Beck T, Sam M, Timms L, Ballin V, Lu Y, Ji J, Zhang X, Chen F, Hu X, Zhou G, Yang Q, Tian G, Zhang L, Xing X, Li X, Zhu Z, Yu Y, Yu J, Yang H, Lathrop M, Tost J, Brennan P, Holcatova I, Zaridze D, Brazma A, Egevard L, Prokhortchouk E, Banks RE, Uhlén M, Cambon-Thomsen A, Viksna J, Ponten F, Skryabin K, Stratton MR, Futreal PA, Birney E, Borg A, Børresen-Dale AL, Caldas C, Foekens JA, Martin S, Reis-Filho JS, Richardson AL, Sotiriou C, Stunnenberg HG, Thoms G, van de Vijver M, van't Veer L, Calvo F, Birnbaum D, Blanche H, Boucher P, Boyault S, Chabannon C, Gut I, Masson-Jacquemier JD, Lathrop M, Pauporté I, Pivot X, Vincent-Salomon A, Tabone E, Theillet C, Thomas G, Tost J, Treilleux I, Calvo F, Bioulac-Sage P, Clément B, Decaens T, Degos F, Franco D, Gut I, Gut M, Heath S, Lathrop M, Samuel D, Thomas G, Zucman-Rossi J, Lichter P, Eils R, Brors B, Korbel JO, Korshunov A, Landgraf P, Lehrach H, Pfister S, Radlwimmer B, Reifenberger G, Taylor MD, von Kalle C, Majumder PP, Sarin R, Rao TS, Bhan MK, Scarpa A, Pederzoli P, Lawlor RA, Delledonne M, Bardelli A, Biankin AV, Grimmond SM, Gress T, Klimstra D, Zamboni G, Shibata T, Nakamura Y, Nakagawa H, Kusada J, Tsunoda T, Miyano S, Aburatani H, Kato K, Fujimoto A, Yoshida T, Campo E, López-Otín C, Estivill X, Guigó R, de Sanjosé S, Piris MA, Montserrat E, González-Díaz M, Puente XS, Jares P, Valencia A, Himmelbauer H, Quesada V, Bea S, Stratton MR, Futreal PA, Campbell PJ, Vincent-Salomon A, Richardson AL, Reis-Filho JS, van de Vijver M, Thomas G, Masson-Jacquemier JD, Aparicio S, Borg A, Børresen-Dale AL, Caldas C, Foekens JA, Stunnenberg HG, van't Veer L, Easton DF, Spellman PT, Martin S, Barker AD, Chin L, Collins FS, Compton CC, Ferguson ML, Gerhard DS, Getz G, Gunter C, Guttmacher A, Guyer M, Hayes DN, Lander ES, Ozenberger B, Penny R, Peterson J, Sander C, Shaw KM, Speed TP, Spellman PT, Vockley JG, Wheeler DA, Wilson RK, Hudson TJ, Chin L, Knoppers BM, Lander ES, Lichter P, Stein LD, Stratton MR, Anderson W, Barker AD, Bell C, Bobrow M, Burke W, Collins FS, Compton CC, DePinho RA, Easton DF, Futreal PA, Gerhard DS, Green AR, Guyer M, Hamilton SR, Hubbard TJ, Kallioniemi OP, Kennedy KL, Ley TJ, Liu ET, Lu Y, Majumder P, Marra M, Ozenberger B, Peterson J, Schafer AJ, Spellman PT, Stunnenberg HG, Wainwright BJ, Wilson RK, Yang H.

Nature. 2010 Apr 15;464(7291):993-8. doi: 10.1038/nature08987. Erratum in: Nature. 2010 Jun 17;465(7300):966. Himmelbaue, Heinz [corrected to Himmelbauer, Heinz]; Gardiner, Brooke A [corrected to Gardiner, Brooke B]; Cross, Anthony [corrected to Cros, Anthony].

21.

Attitudes toward genetic research review: results from a national survey of professionals involved in human subjects protection.

Lemke AA, Trinidad SB, Edwards KL, Starks H, Wiesner GL; GRRIP Consortium.

J Empir Res Hum Res Ethics. 2010 Mar;5(1):83-91. doi: 10.1525/jer.2010.5.1.83.

22.

Developmental defects and childhood cancer.

Slavin TP, Wiesner GL.

Curr Opin Pediatr. 2009 Dec;21(6):717-23. doi: 10.1097/MOP.0b013e328332c612. Review.

PMID:
19812499
23.

Inactivating germ-line and somatic mutations in polypeptide N-acetylgalactosaminyltransferase 12 in human colon cancers.

Guda K, Moinova H, He J, Jamison O, Ravi L, Natale L, Lutterbaugh J, Lawrence E, Lewis S, Willson JK, Lowe JB, Wiesner GL, Parmigiani G, Barnholtz-Sloan J, Dawson DW, Velculescu VE, Kinzler KW, Papadopoulos N, Vogelstein B, Willis J, Gerken TA, Markowitz SD.

Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12921-5. doi: 10.1073/pnas.0901454106. Epub 2009 Jul 17.

24.

Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients.

Guda K, Natale L, Lutterbaugh J, Wiesner GL, Lewis S, Tanner SM, Tomsic J, Valle L, de la Chapelle A, Elston RC, Willis J, Markowitz SD.

Cancer Res. 2009 Jun 15;69(12):4959-61. doi: 10.1158/0008-5472.CAN-09-0225. Epub 2009 Jun 9.

25.

Identification of susceptibility genes for cancer in a genome-wide scan: results from the colon neoplasia sibling study.

Daley D, Lewis S, Platzer P, MacMillen M, Willis J, Elston RC, Markowitz SD, Wiesner GL.

Am J Hum Genet. 2008 Mar;82(3):723-36. doi: 10.1016/j.ajhg.2008.01.007. Epub 2008 Feb 28.

26.

Is TGFBR1*6A a susceptibility allele for nonsyndromic familial colorectal neoplasia?

Daley D, Morgan W, Lewis S, Willis J, Elston RC, Markowitz SD, Wiesner GL.

Cancer Epidemiol Biomarkers Prev. 2007 May;16(5):892-4.

27.

A serious gaming/immersion environment to teach clinical cancer genetics.

Nosek TM, Cohen M, Matthews A, Papp K, Wolf N, Wrenn G, Sher A, Coulter K, Martin J, Wiesner GL.

Stud Health Technol Inform. 2007;125:355-60.

PMID:
17377303
28.

Validation of a self-administered, computerized tool for collecting and displaying the family history of cancer.

Acheson LS, Zyzanski SJ, Stange KC, Deptowicz A, Wiesner GL.

J Clin Oncol. 2006 Dec 1;24(34):5395-402. Epub 2006 Nov 6.

PMID:
17088568
29.

Report of Banbury Summit meeting on training of physicians in medical genetics, October 20-22, 2004.

Korf BR, Feldman G, Wiesner GL.

Genet Med. 2005 Jul-Aug;7(6):433-8. No abstract available.

PMID:
16024976
30.

Identification of Barrett's esophagus in relatives by endoscopic screening.

Chak A, Faulx A, Kinnard M, Brock W, Willis J, Wiesner GL, Parrado AR, Goddard KA.

Am J Gastroenterol. 2004 Nov;99(11):2107-14.

PMID:
15554988
31.

Clinical consult: iron overload--hereditary hemochromatosis.

Matthews AL, Grimes SJ, Wiesner GL, Acheson LS.

Prim Care. 2004 Sep;31(3):767-70, xii-xiii. Review.

PMID:
15331258
32.

Clinical consult: Marfan syndrome.

Grimes SJ, Acheson LS, Matthews AL, Wiesner GL.

Prim Care. 2004 Sep;31(3):739-42, xii. Review.

PMID:
15331256
33.

Cancer genetics in primary care.

Culler D, Grimes SJ, Acheson LS, Wiesner GL.

Prim Care. 2004 Sep;31(3):649-83, xi. Review.

PMID:
15331253
34.

Clinical consult: developmental delay/fragile X syndrome.

Wiesner GL, Cassidy SB, Grimes SJ, Matthews AL, Acheson LS.

Prim Care. 2004 Sep;31(3):621-5, x. Review.

PMID:
15331251
35.

Current and future applications of genetics in primary care medicine.

Acheson LS, Wiesner GL.

Prim Care. 2004 Sep;31(3):449-60, vii. Review.

PMID:
15331241
36.

A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2.

Wiesner GL, Daley D, Lewis S, Ticknor C, Platzer P, Lutterbaugh J, MacMillen M, Baliner B, Willis J, Elston RC, Markowitz SD.

Proc Natl Acad Sci U S A. 2003 Oct 28;100(22):12961-5. Epub 2003 Oct 17.

37.

Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience.

Dugan RB, Wiesner GL, Juengst ET, O'Riordan M, Matthews AL, Robin NH.

Am J Med Genet C Semin Med Genet. 2003 May 15;119C(1):27-34.

PMID:
12704635
38.

Genetic test evaluation: information needs of clinicians, policy makers, and the public.

Burke W, Atkins D, Gwinn M, Guttmacher A, Haddow J, Lau J, Palomaki G, Press N, Richards CS, Wideroff L, Wiesner GL.

Am J Epidemiol. 2002 Aug 15;156(4):311-8. Review.

PMID:
12181100
39.

Reporting BRCA test results to primary care physicians.

Sandhaus LM, Singer ME, Dawson NV, Wiesner GL.

Genet Med. 2001 Sep-Oct;3(5):327-34.

PMID:
11545685
40.

The psychological impact of a negative BRCA1 test: a wolf in sheep's clothing?

Wiesner GL.

Genet Med. 1999 Mar-Apr;1(3):69-70. No abstract available.

PMID:
11336454
41.

Testing for colon neoplasia susceptibility variants at the human COX2 locus.

Wiesner GL, Platzer P, Buxbaum S, Lewis S, MacMillen M, Olechnowicz J, Willis J, Chakravarti A, Elston RC, Markowitz SD.

J Natl Cancer Inst. 2001 Apr 18;93(8):635-9.

PMID:
11309440
42.

Family history-taking in community family practice: implications for genetic screening.

Acheson LS, Wiesner GL, Zyzanski SJ, Goodwin MA, Stange KC.

Genet Med. 2000 May-Jun;2(3):180-5.

PMID:
11256663
43.

Germline BRCA2 mutation in a patient with fallopian tube carcinoma: a case report.

Rose PG, Shrigley R, Wiesner GL.

Gynecol Oncol. 2000 May;77(2):319-20.

PMID:
10785486
44.

Familial gastric cancer: overview and guidelines for management.

Caldas C, Carneiro F, Lynch HT, Yokota J, Wiesner GL, Powell SM, Lewis FR, Huntsman DG, Pharoah PD, Jankowski JA, MacLeod P, Vogelsang H, Keller G, Park KG, Richards FM, Maher ER, Gayther SA, Oliveira C, Grehan N, Wight D, Seruca R, Roviello F, Ponder BA, Jackson CE.

J Med Genet. 1999 Dec;36(12):873-80. Review.

45.

E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer.

Guilford PJ, Hopkins JB, Grady WM, Markowitz SD, Willis J, Lynch H, Rajput A, Wiesner GL, Lindor NM, Burgart LJ, Toro TT, Lee D, Limacher JM, Shaw DW, Findlay MP, Reeve AE.

Hum Mutat. 1999;14(3):249-55.

PMID:
10477433
46.

Cardiac disease in Costello syndrome.

Siwik ES, Zahka KG, Wiesner GL, Limwongse C.

Pediatrics. 1998 Apr;101(4 Pt 1):706-9. Review. No abstract available.

PMID:
9521961
47.

Genetic testing for cancer risk: how to reconcile the conflicts.

Kodish E, Wiesner GL, Mehlman M, Murray T.

JAMA. 1998 Jan 21;279(3):179-81. No abstract available.

PMID:
9438721
48.

Hemihypertrophy. Concepts and controversies.

Ballock RT, Wiesner GL, Myers MT, Thompson GH.

J Bone Joint Surg Am. 1997 Nov;79(11):1731-8. Review. No abstract available.

PMID:
9384434
49.

Clinical implications of BRCA1 genetic testing for Ashkenazi-Jewish women.

Wiesner GL.

Health Matrix Clevel. 1997 Winter;7(1):3-30. No abstract available.

PMID:
10167176
50.

Notification of a family history of breast cancer: issues of privacy and confidentiality.

Winter PR, Wiesner GL, Finnegan J, Bartels D, LeRoy B, Chen PL, Sellers TA.

Am J Med Genet. 1996 Dec 2;66(1):1-6.

PMID:
8957501

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