Mulvihill JJ - Search Results

1

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.

Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M, et al. Zbar B, et al. Among authors: mulvihill jj. Hum Mutat. 1996;8(4):348-57. doi: 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO;2-3. Hum Mutat. 1996. PMID: 8956040

2

Genotype-phenotype correlation in von Hippel-Lindau disease: identification of a mutation associated with VHL type 2A.

Chen F, Slife L, Kishida T, Mulvihill J, Tisherman SE, Zbar B. Chen F, et al. J Med Genet. 1996 Aug;33(8):716-7. doi: 10.1136/jmg.33.8.716. J Med Genet. 1996. PMID: 8863170 Free PMC article.

3

Familial pheochromocytoma due to mutant von Hippel-Lindau disease gene.

Mulvihill JJ, Ferrell RE, Carty SE, Tisherman SE, Zbar B. Mulvihill JJ, et al. Arch Intern Med. 1997 Jun 23;157(12):1390-1. Arch Intern Med. 1997. PMID: 9201016 No abstract available.

4

Three-decade investigation of familial pheochromocytoma. An allele of von Hippel-Lindau disease?

Tisherman SE, Tisherman BG, Tisherman SA, Dunmire S, Levey GS, Mulvihill JJ. Tisherman SE, et al. Among authors: mulvihill jj. Arch Intern Med. 1993 Nov 22;153(22):2550-6. Arch Intern Med. 1993. PMID: 8239848

5

Flanking markers for the gene causing von Recklinghausen neurofibromatosis (NF1).

Seizinger BR, Farmer GE, Haines JL, Ozelius LJ, Anderson K, Korf BR, Parry DM, Pericak-Vance MA, Mulvihill JJ, Menon A, et al. Seizinger BR, et al. Among authors: mulvihill jj. Am J Hum Genet. 1989 Jan;44(1):30-2. Am J Hum Genet. 1989. PMID: 2491778 Free PMC article.

6

What is a gene?

Banke MG, Gettig EA, Rittmeyer LJ, Mulvihill JJ. Banke MG, et al. Among authors: mulvihill jj. Pa Med. 1997 Sep;100(9):24-5. Pa Med. 1997. PMID: 9509866 No abstract available.

7

NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update.

Mulvihill JJ, Parry DM, Sherman JL, Pikus A, Kaiser-Kupfer MI, Eldridge R. Mulvihill JJ, et al. Ann Intern Med. 1990 Jul 1;113(1):39-52. doi: 10.7326/0003-4819-113-1-39. Ann Intern Med. 1990. PMID: 2112353 Review.

8

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.

9

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.

10

Genetic linkage analysis of neurofibromatosis.

Spence MA, Parry DM, Bader JL, Marazita ML, Bocian M, Funderburk SJ, Mulvihill JJ, Sparkes RS. Spence MA, et al. Among authors: mulvihill jj. Ann N Y Acad Sci. 1986;486:287-92. doi: 10.1111/j.1749-6632.1986.tb48081.x. Ann N Y Acad Sci. 1986. PMID: 3105393 No abstract available.

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