Wang Y - Search Results

1

Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia.

Hecht JT, Nelson LD, Crowder E, Wang Y, Elder FF, Harrison WR, Francomano CA, Prange CK, Lennon GG, Deere M, et al. Hecht JT, et al. Among authors: wang y. Nat Genet. 1995 Jul;10(3):325-9. doi: 10.1038/ng0795-325. Nat Genet. 1995. PMID: 7670471

2

Polymorphic dinucleotide repeat in a cartilage matrix protein (CRTM) gene.

Wang Y, Sadler L, Hecht JT. Wang Y, et al. Hum Mol Genet. 1992 Dec;1(9):780. doi: 10.1093/hmg/1.9.780-a. Hum Mol Genet. 1992. PMID: 1302624 No abstract available.

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: wang y. Am J Med Genet. 1992 Nov 1;44(4):420-4. doi: 10.1002/ajmg.1320440406. Am J Med Genet. 1992. PMID: 1442879

4

TaqI and HaeIII RFLP polymorphisms in human proteoglycan link gene (CRTL1).

Hecht JT, Wang Y, Rhodes C, Yamada Y. Hecht JT, et al. Among authors: wang y. Nucleic Acids Res. 1991 Dec 11;19(23):6666. Nucleic Acids Res. 1991. PMID: 1684430 Free PMC article.

5

GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter region.

Hecht JT, Wang Y, Rhodes C, Yamada Y. Hecht JT, et al. Among authors: wang y. Nucleic Acids Res. 1991 Dec 11;19(23):6666. Nucleic Acids Res. 1991. PMID: 1754418 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: wang y. Am J Hum Genet. 1993 Jun;52(6):1230-3. Am J Hum Genet. 1993. PMID: 8099257 Free PMC article.

7

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: wang yp. Am J Hum Genet. 1991 Sep;49(3):682-6. Am J Hum Genet. 1991. PMID: 1679292 Free PMC article.

8

A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1).

Hou J, Parrish J, Lüdecke HJ, Sapru M, Wang Y, Chen W, Hill A, Siegel-Bartelt J, Northrup H, Elder FF, et al. Hou J, et al. Among authors: wang y. Genomics. 1995 Sep 1;29(1):87-97. doi: 10.1006/geno.1995.1218. Genomics. 1995. PMID: 8530105

9

Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.

Hecht JT, Hogue D, Wang Y, Blanton SH, Wagner M, Strong LC, Raskind W, Hansen MF, Wells D. Hecht JT, et al. Among authors: wang y. Am J Hum Genet. 1997 Jan;60(1):80-6. Am J Hum Genet. 1997. PMID: 8981950 Free PMC article.

10

The population-based prevalence of achondroplasia and thanatophoric dysplasia in selected regions of the US.

Waller DK, Correa A, Vo TM, Wang Y, Hobbs C, Langlois PH, Pearson K, Romitti PA, Shaw GM, Hecht JT. Waller DK, et al. Among authors: wang y. Am J Med Genet A. 2008 Sep 15;146A(18):2385-9. doi: 10.1002/ajmg.a.32485. Am J Med Genet A. 2008. PMID: 18698630 Free PMC article.

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