Huff V - Search Results

1

Huff V, Saunders GF. Huff V, et al. Biochim Biophys Acta. 1993 Dec 23;1155(3):295-306. doi: 10.1016/0304-419x(93)90011-z. Biochim Biophys Acta. 1993. PMID: 8268188 Review.

2

RNA expression of the WT1 gene in Wilms' tumors in relation to histology.

Miwa H, Tomlinson GE, Timmons CF, Huff V, Cohn SL, Strong LC, Saunders GF. Miwa H, et al. Among authors: huff v. J Natl Cancer Inst. 1992 Feb 5;84(3):181-7. doi: 10.1093/jnci/84.3.181. J Natl Cancer Inst. 1992. PMID: 1311774

3

Nonlinkage of 16q markers to familial predisposition to Wilms' tumor.

Huff V, Reeve AE, Leppert M, Strong LC, Douglass EC, Geiser CF, Li FP, Meadows A, Callen DF, Lenoir G, et al. Huff V, et al. Cancer Res. 1992 Nov 1;52(21):6117-20. Cancer Res. 1992. PMID: 1356625

4

Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus.

Ton CC, Huff V, Call KM, Cohn S, Strong LC, Housman DE, Saunders GF. Ton CC, et al. Among authors: huff v. Genomics. 1991 May;10(1):293-7. doi: 10.1016/0888-7543(91)90516-h. Genomics. 1991. PMID: 1646159

5

Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT.

Huff V, Miwa H, Haber DA, Call KM, Housman D, Strong LC, Saunders GF. Huff V, et al. Am J Hum Genet. 1991 May;48(5):997-1003. Am J Hum Genet. 1991. PMID: 1673293 Free PMC article.

6

A panel of restriction fragment length polymorphisms for chromosomal band 11p13.

Huff V, Compton DA, Strong LC, Saunders GF. Huff V, et al. Hum Genet. 1990 Feb;84(3):253-7. doi: 10.1007/BF00200570. Hum Genet. 1990. PMID: 1968033

7

An XmnI polymorphism detected by a human genomic clone from chromosomal band 11p13 [D11S416].

Weil MM, Huff V, Compton DA, Strong LC, Saunders GF. Weil MM, et al. Among authors: huff v. Nucleic Acids Res. 1990 Feb 11;18(3):689. doi: 10.1093/nar/18.3.689-a. Nucleic Acids Res. 1990. PMID: 1968626 Free PMC article. No abstract available.

8

A BglII RFLP detected by the probe JA8-1 at human chromosome band 11p13 (D11S417).

Ton CC, Huff V, Weil MM, Strong LC, Saunders GF. Ton CC, et al. Among authors: huff v. Nucleic Acids Res. 1990 Feb 25;18(4):1084. doi: 10.1093/nar/18.4.1084. Nucleic Acids Res. 1990. PMID: 1969141 Free PMC article.

9

Parental origin of de novo constitutional deletions of chromosomal band 11p13.

Huff V, Meadows A, Riccardi VM, Strong LC, Saunders GF. Huff V, et al. Am J Hum Genet. 1990 Jul;47(1):155-60. Am J Hum Genet. 1990. PMID: 1971994 Free PMC article.

10

Familial renal cell carcinoma: hereditary or coincidental?

Levinson AK, Johnson DE, Strong LC, Pathak S, Huff V, Saunders GF. Levinson AK, et al. Among authors: huff v. J Urol. 1990 Oct;144(4):849-51. doi: 10.1016/s0022-5347(17)39607-6. J Urol. 1990. PMID: 2398557

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