Leysens N - Search Results

1

Linkage of inflammatory bowel disease to human chromosome 6p.

Hampe J, Shaw SH, Saiz R, Leysens N, Lantermann A, Mascheretti S, Lynch NJ, MacPherson AJ, Bridger S, van Deventer S, Stokkers P, Morin P, Mirza MM, Forbes A, Lennard-Jones JE, Mathew CG, Curran ME, Schreiber S. Hampe J, et al. Among authors: leysens n. Am J Hum Genet. 1999 Dec;65(6):1647-55. doi: 10.1086/302677. Am J Hum Genet. 1999. PMID: 10577918 Free PMC article.

2

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.

Buetow KH, Shiang R, Yang P, Nakamura Y, Lathrop GM, White R, Wasmuth JJ, Wood S, Berdahl LD, Leysens NJ, et al. Buetow KH, et al. Among authors: leysens nj. Am J Hum Genet. 1991 May;48(5):911-25. Am J Hum Genet. 1991. PMID: 1673289 Free PMC article.

3

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC. Lidral AC, et al. Among authors: leysens nj. Am J Hum Genet. 1998 Aug;63(2):557-68. doi: 10.1086/301956. Am J Hum Genet. 1998. PMID: 9683588 Free PMC article.

4

Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus.

Semina EV, Datson NA, Leysens NJ, Zabel BU, Carey JC, Bell GI, Bitoun P, Lindgren C, Stevenson T, Frants RR, van Ommen G, Murray JC. Semina EV, et al. Among authors: leysens nj. Am J Hum Genet. 1996 Dec;59(6):1288-96. Am J Hum Genet. 1996. PMID: 8940274 Free PMC article.

5

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.

Semina EV, Reiter R, Leysens NJ, Alward WL, Small KW, Datson NA, Siegel-Bartelt J, Bierke-Nelson D, Bitoun P, Zabel BU, Carey JC, Murray JC. Semina EV, et al. Among authors: leysens nj. Nat Genet. 1996 Dec;14(4):392-9. doi: 10.1038/ng1296-392. Nat Genet. 1996. PMID: 8944018

6

Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes.

Yoshiura K, Leysens NJ, Chang J, Ward D, Murray JC, Muenke M. Yoshiura K, et al. Among authors: leysens nj. Am J Med Genet. 1997 Oct 31;72(3):354-62. Am J Med Genet. 1997. PMID: 9332670

7

A KpnI polymorphism for the human insulin-responsive glucose transporter gene (GLUT4) on chromosome 17.

Leysens N, Murray JC, Bell GI. Leysens N, et al. Nucleic Acids Res. 1989 May 11;17(9):3621. doi: 10.1093/nar/17.9.3621. Nucleic Acids Res. 1989. PMID: 2566978 Free PMC article.

8

A dinucleotide repeat for the D1S53 locus.

Nishimura DY, Leysens NJ, Murray JC. Nishimura DY, et al. Among authors: leysens nj. Nucleic Acids Res. 1992 Mar 11;20(5):1167. Nucleic Acids Res. 1992. PMID: 1549502 Free PMC article.

9

Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family.

Stadler HS, Murray JC, Leysens NJ, Goodfellow PJ, Solursh M. Stadler HS, et al. Among authors: leysens nj. Mamm Genome. 1995 Jun;6(6):383-8. doi: 10.1007/BF00355637. Mamm Genome. 1995. PMID: 7647458

10

Exclusion of Ifa and Ifb as the Lps gene and mapping of three markers near the Lps locus.

Peiffer-Schneider S, Schutte BC, Murray JC, Frees KL, Williamson K, Leysens NJ, Schwartz DA. Peiffer-Schneider S, et al. Among authors: leysens nj. Mamm Genome. 1997 Oct;8(10):785-6. doi: 10.1007/s003359900569. Mamm Genome. 1997. PMID: 9321479 No abstract available.

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