Goodfellow PJ - Search Results

1

Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q.

Kwon JM, Elliott JL, Yee WC, Ivanovich J, Scavarda NJ, Moolsintong PJ, Goodfellow PJ. Kwon JM, et al. Among authors: goodfellow pj. Am J Hum Genet. 1995 Oct;57(4):853-8. Am J Hum Genet. 1995. PMID: 7573046 Free PMC article.

2

Genetic analysis of kifafa, a complex familial seizure disorder.

Neuman RJ, Kwon JM, Jilek-Aall L, Rwiza HT, Rice JP, Goodfellow PJ. Neuman RJ, et al. Among authors: goodfellow pj. Am J Hum Genet. 1995 Oct;57(4):902-10. Am J Hum Genet. 1995. PMID: 7573052 Free PMC article.

3

Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics.

Elliott JL, Kwon JM, Goodfellow PJ, Yee WC. Elliott JL, et al. Among authors: goodfellow pj. Neurology. 1997 Jan;48(1):23-8. doi: 10.1212/wnl.48.1.23. Neurology. 1997. PMID: 9008488

4

Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B.

Kitamura Y, Scavarda N, Wells SA Jr, Jackson CE, Goodfellow PJ. Kitamura Y, et al. Among authors: goodfellow pj. Hum Mol Genet. 1995 Oct;4(10):1987-8. doi: 10.1093/hmg/4.10.1987. Hum Mol Genet. 1995. PMID: 8595427 No abstract available.

5

Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.

Kaphingst KA, Ivanovich J, Biesecker BB, Dresser R, Seo J, Dressler LG, Goodfellow PJ, Goodman MS. Kaphingst KA, et al. Among authors: goodfellow pj. Clin Genet. 2016 Mar;89(3):378-84. doi: 10.1111/cge.12597. Epub 2015 May 5. Clin Genet. 2016. PMID: 25871653 Free PMC article.

6

MSI in endometrial carcinoma: absence of MLH1 promoter methylation is associated with increased familial risk for cancers.

Whelan AJ, Babb S, Mutch DG, Rader J, Herzog TJ, Todd C, Ivanovich JL, Goodfellow PJ. Whelan AJ, et al. Among authors: goodfellow pj. Int J Cancer. 2002 Jun 10;99(5):697-704. doi: 10.1002/ijc.10429. Int J Cancer. 2002. PMID: 12115503

7

Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.

Carlson KM, Dou S, Chi D, Scavarda N, Toshima K, Jackson CE, Wells SA Jr, Goodfellow PJ, Donis-Keller H. Carlson KM, et al. Among authors: goodfellow pj. Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1579-83. doi: 10.1073/pnas.91.4.1579. Proc Natl Acad Sci U S A. 1994. PMID: 7906417 Free PMC article.

8

Frequent deletion of chromosome 1p sequences in an aggressive histologic subtype of endometrial cancer.

Arlt MF, Herzog TJ, Mutch DG, Gersell DJ, Liu H, Goodfellow PJ. Arlt MF, et al. Among authors: goodfellow pj. Hum Mol Genet. 1996 Jul;5(7):1017-21. doi: 10.1093/hmg/5.7.1017. Hum Mol Genet. 1996. PMID: 8817340

9

Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability.

Herfarth KK, Kodner IJ, Whelan AJ, Ivanovich JL, Bracamontes JR, Wells SA Jr, Goodfellow PJ. Herfarth KK, et al. Among authors: goodfellow pj. Genes Chromosomes Cancer. 1997 Jan;18(1):42-9. doi: 10.1002/(sici)1098-2264(199701)18:1<42::aid-gcc5>3.0.co;2-1. Genes Chromosomes Cancer. 1997. PMID: 8993979

10

MonoSeq Variant Caller Reveals Novel Mononucleotide Run Indel Mutations in Tumors with Defective DNA Mismatch Repair.

Walker CJ, Miranda MA, O'Hern MJ, Blachly JS, Moyer CL, Ivanovich J, Kroll KW, Eisfeld AK, Sapp CE, Mutch DG, Cohn DE, Bundschuh R, Goodfellow PJ. Walker CJ, et al. Among authors: goodfellow pj. Hum Mutat. 2016 Oct;37(10):1004-12. doi: 10.1002/humu.23036. Epub 2016 Aug 8. Hum Mutat. 2016. PMID: 27346418 Free PMC article.

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