Hecht JT - Search Results

1

Genomic characterization of human DSPG3.

Deere M, Dieguez JL, Yoon SJ, Hewett-Emmett D, de la Chapelle A, Hecht JT. Deere M, et al. Among authors: hecht jt. Genome Res. 1999 May;9(5):449-56. Genome Res. 1999. PMID: 10330124 Free PMC article.

2

Characterization of human DSPG3, a small dermatan sulfate proteoglycan.

Deere M, Johnson J, Garza S, Harrison WR, Yoon SJ, Elder FF, Kucherlapati R, Hook M, Hecht JT. Deere M, et al. Among authors: hecht jt. Genomics. 1996 Dec 15;38(3):399-404. doi: 10.1006/geno.1996.0643. Genomics. 1996. PMID: 8975717

3

Characterization of cartilage oligomeric matrix protein (COMP) in human normal and pseudoachondroplasia musculoskeletal tissues.

Hecht JT, Deere M, Putnam E, Cole W, Vertel B, Chen H, Lawler J. Hecht JT, et al. Matrix Biol. 1998 Aug;17(4):269-78. doi: 10.1016/s0945-053x(98)90080-4. Matrix Biol. 1998. PMID: 9749943

4

Analysis of the promoter region of human cartilage oligomeric matrix protein (COMP).

Deere M, Rhoades Hall C, Gunning KB, LeFebvre V, Ridall AL, Hecht JT. Deere M, et al. Among authors: hecht jt. Matrix Biol. 2001 Jan;19(8):783-92. doi: 10.1016/s0945-053x(00)00127-x. Matrix Biol. 2001. PMID: 11223338

5

Mosaicism in pseudoachondroplasia.

Ferguson HL, Deere M, Evans R, Rotta J, Hall JG, Hecht JT. Ferguson HL, et al. Among authors: hecht jt. Am J Med Genet. 1997 Jun 13;70(3):287-91. Am J Med Genet. 1997. PMID: 9188668

6

Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia.

Deere M, Sanford T, Ferguson HL, Daniels K, Hecht JT. Deere M, et al. Among authors: hecht jt. Am J Med Genet. 1998 Dec 28;80(5):510-3. doi: 10.1002/(sici)1096-8628(19981228)80:5<510::aid-ajmg14>3.0.co;2-f. Am J Med Genet. 1998. PMID: 9880218

7

Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasia.

Deere M, Sanford T, Francomano CA, Daniels K, Hecht JT. Deere M, et al. Among authors: hecht jt. Am J Med Genet. 1999 Aug 27;85(5):486-90. doi: 10.1002/(sici)1096-8628(19990827)85:5<486::aid-ajmg10>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10405447

8

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. Nat Genet. 1995 Jul;10(3):325-9. doi: 10.1038/ng0795-325. Nat Genet. 1995. PMID: 7670471

9

Genetic heterogeneity in multiple epiphyseal dysplasia.

Deere M, Blanton SH, Scott CI, Langer LO, Pauli RM, Hecht JT. Deere M, et al. Among authors: hecht jt. Am J Hum Genet. 1995 Mar;56(3):698-704. Am J Hum Genet. 1995. PMID: 7887425 Free PMC article.

10

Linkage of typical pseudoachondroplasia to chromosome 19.

Hecht JT, Francomano CA, Briggs MD, Deere M, Conner B, Horton WA, Warman M, Cohn DH, Blanton SH. Hecht JT, et al. Genomics. 1993 Dec;18(3):661-6. doi: 10.1016/s0888-7543(05)80370-2. Genomics. 1993. PMID: 8307577

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