Huff V - Search Results

1

Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31.

Szabó J, Heath B, Hill VM, Jackson CE, Zarbo RJ, Mallette LE, Chew SL, Besser GM, Thakker RV, Huff V, et al. Szabó J, et al. Among authors: huff v. Am J Hum Genet. 1995 Apr;56(4):944-50. Am J Hum Genet. 1995. PMID: 7717405 Free PMC article.

2

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.

3

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.

4

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

5

Familial Wilms tumor.

Ruteshouser EC, Huff V. Ruteshouser EC, et al. Among authors: huff v. Am J Med Genet C Semin Med Genet. 2004 Aug 15;129C(1):29-34. doi: 10.1002/ajmg.c.30025. Am J Med Genet C Semin Med Genet. 2004. PMID: 15264270 Review.

6

WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences.

Huff V, Jaffe N, Saunders GF, Strong LC, Villalba F, Ruteshouser EC. Huff V, et al. Am J Hum Genet. 1995 Jan;56(1):84-90. Am J Hum Genet. 1995. PMID: 7825606 Free PMC article.

7

Wilms tumor genetics.

Huff V. Huff V. Am J Med Genet. 1998 Oct 2;79(4):260-7. doi: 10.1002/(sici)1096-8628(19981002)79:4<260::aid-ajmg6>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9781905 Review.

8

Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18.

Anderson CE, Punnett HH, Huff V, de Chadarévian JP. Anderson CE, et al. Among authors: huff v. Am J Med Genet A. 2003 Aug 15;121A(1):52-5. doi: 10.1002/ajmg.a.20141. Am J Med Genet A. 2003. PMID: 12900902

9

Familial Wilms' tumor with neural elements: characterization by histology, immunohistochemistry, and genetic analysis.

Hussong JW, Perkins SL, Huff V, McDonald JM, Pysher TJ, Beckwith JB, Coffin CM. Hussong JW, et al. Among authors: huff v. Pediatr Dev Pathol. 2000 Nov-Dec;3(6):561-7. doi: 10.1007/s100240010106. Pediatr Dev Pathol. 2000. PMID: 11000334

10

Genetic mosaicism in normal tissues of Wilms' tumour patients.

Chao LY, Huff V, Tomlinson G, Riccardi VM, Strong LC, Saunders GF. Chao LY, et al. Among authors: huff v. Nat Genet. 1993 Feb;3(2):127-31. doi: 10.1038/ng0293-127. Nat Genet. 1993. PMID: 8388768

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