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Medical geneticists confront ethical dilemmas: cross-cultural comparisons among 18 nations.
Wertz DC, Fletcher JC, Mulvihill JJ. Wertz DC, et al. Among authors: mulvihill jj. Am J Hum Genet. 1990 Jun;46(6):1200-13. Am J Hum Genet. 1990. PMID: 2339711 Free PMC article.
Strategies for controlling cancer through genetics: report of a workshop.
Parry DM, Berg K, Mulvihill JJ, Carter CL, Miller RW. Parry DM, et al. Among authors: mulvihill jj. Am J Hum Genet. 1987 Jul;41(1):63-9. Am J Hum Genet. 1987. PMID: 3605097 Free PMC article. No abstract available.
Further delineation of the Baller-Gerold syndrome.
Lin AE, McPherson E, Nwokoro NA, Clemens M, Losken HW, Mulvihill JJ. Lin AE, et al. Among authors: mulvihill jj. Am J Med Genet. 1993 Feb 15;45(4):519-24. doi: 10.1002/ajmg.1320450423. Am J Med Genet. 1993. PMID: 8465861 Review.
Inheritance of acute appendicitis: familial aggregation and evidence of polygenic transmission.
Basta M, Morton NE, Mulvihill JJ, Radovanović Z, Radojicić C, Marinković D. Basta M, et al. Among authors: mulvihill jj. Am J Hum Genet. 1990 Feb;46(2):377-82. Am J Hum Genet. 1990. PMID: 2301403 Free PMC article.
Reported environmental exposures are inversely associated with obtaining a genetic diagnosis in the Undiagnosed Diseases Network.
Silverman EK, Allard P, Loscalzo J, Mulvihill JJ, Korrick SA; Undiagnosed Diseases Network. Silverman EK, et al. Among authors: mulvihill jj. Am J Med Genet A. 2019 Jun;179(6):958-965. doi: 10.1002/ajmg.a.61132. Epub 2019 Mar 23. Am J Med Genet A. 2019. PMID: 30903737
Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.
Goldgar DE, Green P, Parry DM, Mulvihill JJ. Goldgar DE, et al. Among authors: mulvihill jj. Am J Hum Genet. 1989 Jan;44(1):6-12. Am J Hum Genet. 1989. PMID: 2491784 Free PMC article.
The Bell Curve: statement by the NIH-DOE Joint Working Group on the Ethical, Legal, and Social Implications of Human Genome Research.
Allen A, Anderson B, Andrews L, Beckwith J, Bowman J, Cook-Deegan R, Cox D, Duster T, Eisenberg R, Fine B, Holtzman N, King P, Kitcher P, McInerney J, McKusick V, Mulvihill J, Murray J, Murray R, Murray T, Nelkin D, Rapp R, Saxton M, Wexler N. Allen A, et al. Among authors: mulvihill j. Am J Hum Genet. 1996 Aug;59(2):487-8. Am J Hum Genet. 1996. PMID: 8755944 Free PMC article. No abstract available.
The floating harbor syndrome with cardiac septal defect.
Lazebnik N, McPherson E, Rittmeyer LJ, Mulvihill JJ. Lazebnik N, et al. Among authors: mulvihill jj. Am J Med Genet. 1996 Dec 18;66(3):300-2. doi: 10.1002/(SICI)1096-8628(19961218)66:3<300::AID-AJMG12>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8985491 Review.
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.
Muenke M, Gripp KW, McDonald-McGinn DM, Gaudenz K, Whitaker LA, Bartlett SP, Markowitz RI, Robin NH, Nwokoro N, Mulvihill JJ, Losken HW, Mulliken JB, Guttmacher AE, Wilroy RS, Clarke LA, Hollway G, Adès LC, Haan EA, Mulley JC, Cohen MM Jr, Bellus GA, Francomano CA, Moloney DM, Wall SA, Wilkie AO, et al. Muenke M, et al. Among authors: mulvihill jj. Am J Hum Genet. 1997 Mar;60(3):555-64. Am J Hum Genet. 1997. PMID: 9042914 Free PMC article.
Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications.
Andersson HC, Parry DM, Mulvihill JJ. Andersson HC, et al. Among authors: mulvihill jj. Am J Med Genet. 1995 Mar 13;56(1):72-5. doi: 10.1002/ajmg.1320560116. Am J Med Genet. 1995. PMID: 7747790 Review.
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