Bray-Ward P - Search Results

1

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome.

Hobart HH, Morris CA, Mervis CB, Pani AM, Kistler DJ, Rios CM, Kimberley KW, Gregg RG, Bray-Ward P. Hobart HH, et al. Among authors: bray ward p. Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):220-8. doi: 10.1002/ajmg.c.30258. Am J Med Genet C Semin Med Genet. 2010. PMID: 20425783 Free PMC article.

2

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.

Pani AM, Hobart HH, Morris CA, Mervis CB, Bray-Ward P, Kimberley KW, Rios CM, Clark RC, Gulbronson MD, Gowans GC, Gregg RG. Pani AM, et al. Among authors: bray ward p. PLoS One. 2010 Aug 31;5(8):e12349. doi: 10.1371/journal.pone.0012349. PLoS One. 2010. PMID: 20824207 Free PMC article.

3

Generation of an inbred miniature pig model of retinitis pigmentosa.

Ross JW, Fernandez de Castro JP, Zhao J, Samuel M, Walters E, Rios C, Bray-Ward P, Jones BW, Marc RE, Wang W, Zhou L, Noel JM, McCall MA, DeMarco PJ, Prather RS, Kaplan HJ. Ross JW, et al. Among authors: bray ward p. Invest Ophthalmol Vis Sci. 2012 Jan 31;53(1):501-7. doi: 10.1167/iovs.11-8784. Invest Ophthalmol Vis Sci. 2012. PMID: 22247487 Free PMC article.

4

The human HNRPD locus maps to 4q21 and encodes a highly conserved protein.

Dempsey LA, Li MJ, DePace A, Bray-Ward P, Maizels N. Dempsey LA, et al. Genomics. 1998 May 1;49(3):378-84. doi: 10.1006/geno.1998.5237. Genomics. 1998. PMID: 9615222 Free article.

5

Comprehensive human genome amplification using multiple displacement amplification.

Dean FB, Hosono S, Fang L, Wu X, Faruqi AF, Bray-Ward P, Sun Z, Zong Q, Du Y, Du J, Driscoll M, Song W, Kingsmore SF, Egholm M, Lasken RS. Dean FB, et al. Among authors: bray ward p. Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5261-6. doi: 10.1073/pnas.082089499. Proc Natl Acad Sci U S A. 2002. PMID: 11959976 Free PMC article.

6

Molecular cloning of a zinc finger gene eZNF from a human inner ear cDNA library, and in situ expression pattern of its mouse homologue in mouse inner ear.

Jacob AN, Manjunath NA, Bray-Ward P, Kandpal RP. Jacob AN, et al. Somat Cell Mol Genet. 1998 Mar;24(2):121-9. doi: 10.1023/b:scam.0000007114.14371.f4. Somat Cell Mol Genet. 1998. PMID: 9919311

7

Genomic localization of the human gene for KCNA10, a cGMP-activated K channel.

Orias M, Bray-Ward P, Curran ME, Keating MT, Desir GV. Orias M, et al. Genomics. 1997 May 15;42(1):33-7. doi: 10.1006/geno.1997.4712. Genomics. 1997. PMID: 9177773 Free article.

8

A transcription map of the major histocompatibility complex (MHC) class I region.

Gruen JR, Nalabolu SR, Chu TW, Bowlus C, Fan WF, Goei VL, Wei H, Sivakamasundari R, Liu Y, Xu HX, Parimoo S, Nallur G, Ajioka R, Shukla H, Bray-Ward P, Pan J, Weissman SM. Gruen JR, et al. Genomics. 1996 Aug 15;36(1):70-85. doi: 10.1006/geno.1996.0427. Genomics. 1996. PMID: 8812418 Free article.

9

Characteristics of three homologous 202 genes (Ifi202a, Ifi202b, and Ifi202c) from the murine interferon-activatable gene 200 cluster.

Wang H, Chatterjee G, Meyer JJ, Liu CJ, Manjunath NA, Bray-Ward P, Lengyel P. Wang H, et al. Genomics. 1999 Sep 15;60(3):281-94. doi: 10.1006/geno.1999.5923. Genomics. 1999. PMID: 10493828 Free article.

10

FISH-Mapped CEPH YACs spanning 0 to 46 cM on human chromosome 6.

Bray-Ward P, Bowlus C, Choi J, Paslier DL, Weissenbach J, Gruen JR. Bray-Ward P, et al. Genomics. 1996 Aug 15;36(1):104-11. doi: 10.1006/geno.1996.0430. Genomics. 1996. PMID: 8812421 Free article.

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