Scherer SW - Search Results

1

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW. Zeesman S, et al. Among authors: scherer sw. Am J Med Genet A. 2006 Mar 1;140(5):509-14. doi: 10.1002/ajmg.a.31110. Am J Med Genet A. 2006. PMID: 16470794

2

Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient.

Alley TL, Gray BA, Lee SH, Scherer SW, Tsui LC, Tint GS, Williams CA, Zori R, Wallace MR. Alley TL, et al. Among authors: scherer sw. Am J Hum Genet. 1995 Jun;56(6):1411-6. Am J Hum Genet. 1995. PMID: 7762564 Free PMC article.

3

Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia.

Johnson EJ, Scherer SW, Osborne L, Tsui LC, Oscier D, Mould S, Cotter FE. Johnson EJ, et al. Among authors: scherer sw. Blood. 1996 May 1;87(9):3579-86. Blood. 1996. PMID: 8611680 Free article.

4

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.

Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC. Osborne LR, et al. Among authors: scherer sw. Genomics. 1996 Sep 1;36(2):328-36. doi: 10.1006/geno.1996.0469. Genomics. 1996. PMID: 8812460 Free article.

5

Fine mapping of the human and mouse genes for the type I procollagen COOH-terminal proteinase enhancer protein.

Takahara K, Osborne L, Elliott RW, Tsui LC, Scherer SW, Greenspan DS. Takahara K, et al. Among authors: scherer sw. Genomics. 1996 Jan 15;31(2):253-6. doi: 10.1006/geno.1996.0043. Genomics. 1996. PMID: 8824813

6

Physical mapping of the chromosome 7 breakpoint region in an SLOS patient with t(7;20) (q32.1;q13.2).

Alley TL, Scherer SW, Huizenga JJ, Tsui LC, Wallace MR. Alley TL, et al. Among authors: scherer sw. Am J Med Genet. 1997 Jan 31;68(3):279-81. Am J Med Genet. 1997. PMID: 9024559

7

Resources for human genetics on the World Wide Web.

Osborne LR, Lee JR, Scherer SW. Osborne LR, et al. Among authors: scherer sw. Mol Med Today. 1997 Sep;3(9):370-3. doi: 10.1016/S1357-4310(97)82918-8. Mol Med Today. 1997. PMID: 9302686

8

Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome.

Osborne LR, Soder S, Shi XM, Pober B, Costa T, Scherer SW, Tsui LC. Osborne LR, et al. Among authors: scherer sw. Am J Hum Genet. 1997 Aug;61(2):449-52. doi: 10.1086/514850. Am J Hum Genet. 1997. PMID: 9311751 Free PMC article. No abstract available.

9

Osborne LR, Herbrick JA, Greavette T, Heng HH, Tsui LC, Scherer SW. Osborne LR, et al. Among authors: scherer sw. Genomics. 1997 Oct 15;45(2):402-6. doi: 10.1006/geno.1997.4923. Genomics. 1997. PMID: 9344666

10

The BCL7 gene family: deletion of BCL7B in Williams syndrome.

Jadayel DM, Osborne LR, Coignet LJ, Zani VJ, Tsui LC, Scherer SW, Dyer MJ. Jadayel DM, et al. Among authors: scherer sw. Gene. 1998 Dec 11;224(1-2):35-44. doi: 10.1016/s0378-1119(98)00514-9. Gene. 1998. PMID: 9931421

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