Lee B - Search Results

1

Characterization of the human HOX 7 cDNA and identification of polymorphic markers.

Padanilam BJ, Stadler HS, Mills KA, McLeod LB, Solursh M, Lee B, Ramirez F, Buetow KH, Murray JC. Padanilam BJ, et al. Among authors: lee b. Hum Mol Genet. 1992 Sep;1(6):407-10. doi: 10.1093/hmg/1.6.407. Hum Mol Genet. 1992. PMID: 1284527

2

Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis.

Horton WA, Machado MA, Ellard J, Campbell D, Bartley J, Ramirez F, Vitale E, Lee B. Horton WA, et al. Among authors: lee b. Proc Natl Acad Sci U S A. 1992 May 15;89(10):4583-7. doi: 10.1073/pnas.89.10.4583. Proc Natl Acad Sci U S A. 1992. PMID: 1374906 Free PMC article.

3

Clinical and genetic associations in Marfan syndrome and related disorders.

Ramirez F, Lee B, Vitale E. Ramirez F, et al. Among authors: lee b. Mt Sinai J Med. 1992 Sep;59(4):350-6. Mt Sinai J Med. 1992. PMID: 1406753

4

G to T transversion at position +5 of a splice donor site causes skipping of the preceding exon in the type III procollagen transcripts of a patient with Ehlers-Danlos syndrome type IV.

Lee B, Vitale E, Superti-Furga A, Steinmann B, Ramirez F. Lee B, et al. J Biol Chem. 1991 Mar 15;266(8):5256-9. J Biol Chem. 1991. PMID: 1672129 Free article.

5

Modifications in the organization and expression of collagen genes associated with skeletal disorders.

Lee B, D'Alessio M, Ramirez F. Lee B, et al. Crit Rev Eukaryot Gene Expr. 1991;1(3):173-87. Crit Rev Eukaryot Gene Expr. 1991. PMID: 1802109 Review.

6

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes.

Lee B, Godfrey M, Vitale E, Hori H, Mattei MG, Sarfarazi M, Tsipouras P, Ramirez F, Hollister DW. Lee B, et al. Nature. 1991 Jul 25;352(6333):330-4. doi: 10.1038/352330a0. Nature. 1991. PMID: 1852206

7

Marshall syndrome.

Stratton RF, Lee B, Ramirez F. Stratton RF, et al. Among authors: lee b. Am J Med Genet. 1991 Oct 1;41(1):35-8. doi: 10.1002/ajmg.1320410111. Am J Med Genet. 1991. PMID: 1951461

8

A glycine to serine polymorphism in the C-propeptide of the human type II procollagen.

Vissing H, Rasmussen M, D'Alessio M, Lee B, Dobkin C, Ramirez F. Vissing H, et al. Among authors: lee b. Nucleic Acids Res. 1990 Jun 11;18(11):3431. doi: 10.1093/nar/18.11.3431. Nucleic Acids Res. 1990. PMID: 1972570 Free PMC article.

9

Characterization of a large deletion associated with a polymorphic block of repeated dinucleotides in the type III procollagen gene (COL3A1) of a patient with Ehlers-Danlos syndrome type IV.

Lee B, D'Alessio M, Vissing H, Ramirez F, Steinmann B, Superti-Furga A. Lee B, et al. Am J Hum Genet. 1991 Mar;48(3):511-7. Am J Hum Genet. 1991. PMID: 1998337 Free PMC article.

10

Multiexon deletion in the procollagen III gene is associated with mild Ehlers-Danlos syndrome type IV.

Vissing H, D'Alessio M, Lee B, Ramirez F, Byers PH, Steinmann B, Superti-Furga A. Vissing H, et al. Among authors: lee b. J Biol Chem. 1991 Mar 15;266(8):5244-8. J Biol Chem. 1991. PMID: 2002056 Free article.

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