Daiger SP - Search Results

1

Cleft lip and palate: no evidence of linkage to transforming growth factor alpha.

Hecht JT, Wang YP, Blanton SH, Michels VV, Daiger SP. Hecht JT, et al. Among authors: daiger sp. Am J Hum Genet. 1991 Sep;49(3):682-6. Am J Hum Genet. 1991. PMID: 1679292 Free PMC article.

2

Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere.

Northrup H, Kwiatkowski DJ, Roach ES, Dobyns WB, Lewis RA, Herman GE, Rodriguez E Jr, Daiger SP, Blanton SH. Northrup H, et al. Among authors: daiger sp. Am J Hum Genet. 1992 Oct;51(4):709-20. Am J Hum Genet. 1992. PMID: 1415216 Free PMC article.

3

Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasia.

Hecht JT, Blanton SH, Wang Y, Daiger SP, Horton WA, Rhodes C, Yamada Y, Francomano CA. Hecht JT, et al. Among authors: daiger sp. Am J Med Genet. 1992 Nov 1;44(4):420-4. doi: 10.1002/ajmg.1320440406. Am J Med Genet. 1992. PMID: 1442879

4

Van der Woude syndrome and nonsyndromic cleft lip and palate.

Hecht JT, Wang Y, Blanton SH, Daiger SP. Hecht JT, et al. Among authors: daiger sp. Am J Hum Genet. 1992 Aug;51(2):442-4. Am J Hum Genet. 1992. PMID: 1642245 Free PMC article. No abstract available.

5

X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

McGuire RE, Sullivan LS, Blanton SH, Church MW, Heckenlively JR, Daiger SP. McGuire RE, et al. Among authors: daiger sp. Am J Hum Genet. 1995 Jul;57(1):87-94. Am J Hum Genet. 1995. PMID: 7611300 Free PMC article.

6

Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A.

Hecht JT, Wang Y, Connor B, Blanton SH, Daiger SP. Hecht JT, et al. Among authors: daiger sp. Am J Hum Genet. 1993 Jun;52(6):1230-3. Am J Hum Genet. 1993. PMID: 8099257 Free PMC article.

7

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.

Bowne SJ, Sullivan LS, Blanton SH, Cepko CL, Blackshaw S, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP. Bowne SJ, et al. Among authors: daiger sp. Hum Mol Genet. 2002 Mar 1;11(5):559-68. doi: 10.1093/hmg/11.5.559. Hum Mol Genet. 2002. PMID: 11875050 Free PMC article.

8

A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement.

Bowne SJ, Humphries MM, Sullivan LS, Kenna PF, Tam LC, Kiang AS, Campbell M, Weinstock GM, Koboldt DC, Ding L, Fulton RS, Sodergren EJ, Allman D, Millington-Ward S, Palfi A, McKee A, Blanton SH, Slifer S, Konidari I, Farrar GJ, Daiger SP, Humphries P. Bowne SJ, et al. Among authors: daiger sp. Eur J Hum Genet. 2011 Oct;19(10):1074-81. doi: 10.1038/ejhg.2011.86. Epub 2011 Jun 8. Eur J Hum Genet. 2011. PMID: 21654732 Free PMC article.

9

Exome-based mapping and variant prioritization for inherited Mendelian disorders.

Koboldt DC, Larson DE, Sullivan LS, Bowne SJ, Steinberg KM, Churchill JD, Buhr AC, Nutter N, Pierce EA, Blanton SH, Weinstock GM, Wilson RK, Daiger SP. Koboldt DC, et al. Among authors: daiger sp. Am J Hum Genet. 2014 Mar 6;94(3):373-84. doi: 10.1016/j.ajhg.2014.01.016. Epub 2014 Feb 20. Am J Hum Genet. 2014. PMID: 24560519 Free PMC article.

10

A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13.

Cottingham AW, Sadler LA, Blanton SH, Wagner MJ, Wells DE, Heckenlively JR, Daiger SP. Cottingham AW, et al. Among authors: daiger sp. Nucleic Acids Res. 1992 Mar 25;20(6):1426. doi: 10.1093/nar/20.6.1426. Nucleic Acids Res. 1992. PMID: 1348578 Free PMC article.

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