Li X - Search Results

1

Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3.

Jabs EW, Li X, Coss CA, Taylor EW, Meyers DA, Weber JL. Jabs EW, et al. Among authors: li x. Genomics. 1991 Sep;11(1):193-8. Genomics. 1991. PMID: 1765376

2

Molecular cloning, chromosomal mapping, and characterization of the mouse UDP-galactose:ceramide galactosyltransferase gene.

Coetzee T, Li X, Fujita N, Marcus J, Suzuki K, Francke U, Popko B. Coetzee T, et al. Among authors: li x. Genomics. 1996 Jul 1;35(1):215-22. doi: 10.1006/geno.1996.0341. Genomics. 1996. PMID: 8661123

3

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.

Jabs EW, Li X, Scott AF, Meyers G, Chen W, Eccles M, Mao JI, Charnas LR, Jackson CE, Jaye M. Jabs EW, et al. Among authors: li x. Nat Genet. 1994 Nov;8(3):275-9. doi: 10.1038/ng1194-275. Nat Genet. 1994. PMID: 7874170

4

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis.

Jabs EW, Müller U, Li X, Ma L, Luo W, Haworth IS, Klisak I, Sparkes R, Warman ML, Mulliken JB, et al. Jabs EW, et al. Among authors: li x. Cell. 1993 Nov 5;75(3):443-50. doi: 10.1016/0092-8674(93)90379-5. Cell. 1993. PMID: 8106171

5

Physical and genetic mapping of a human apical epithelial Na+/H+ exchanger (NHE3) isoform to chromosome 5p15.3.

Brant SR, Bernstein M, Wasmuth JJ, Taylor EW, McPherson JD, Li X, Walker S, Pouyssegur J, Donowitz M, Tse CM, et al. Brant SR, et al. Among authors: li x. Genomics. 1993 Mar;15(3):668-72. doi: 10.1006/geno.1993.1122. Genomics. 1993. PMID: 8096830

6

Localization of the human Mxi1 transcription factor gene (MXI1) to chromosome 10q24-q25.

Wechsler DS, Hawkins AL, Li X, Jabs EW, Griffin CA, Dang CV. Wechsler DS, et al. Among authors: li x. Genomics. 1994 Jun;21(3):669-72. doi: 10.1006/geno.1994.1336. Genomics. 1994. PMID: 7959753 No abstract available.

7

Backfoot, a novel homeobox gene, maps to human chromosome 5 (BFT) and mouse chromosome 13 (Bft).

Shang J, Li X, Ring HZ, Clayton DA, Francke U. Shang J, et al. Among authors: li x. Genomics. 1997 Feb 15;40(1):108-13. doi: 10.1006/geno.1996.4558. Genomics. 1997. PMID: 9070926

8

High-density radiation hybrid map of human chromosome 18 and contig of 18p.

Giacalone J, Li X, Lehrach H, Francke U. Giacalone J, et al. Among authors: li x. Genomics. 1996 Oct 1;37(1):9-18. doi: 10.1006/geno.1996.0514. Genomics. 1996. PMID: 8921364

9

The IPP gene is assigned to human chromosome 1p32-1p22.

Chang-Yeh A, Jabs EW, Li X, Dracopoli NC, Huang RC. Chang-Yeh A, et al. Among authors: li x. Genomics. 1993 Jan;15(1):239-41. doi: 10.1006/geno.1993.1048. Genomics. 1993. PMID: 8432546 No abstract available.

10

Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18.

Li X, Pereira L, Zhang H, Sanguineti C, Ramirez F, Bonadio J, Francke U. Li X, et al. Genomics. 1993 Dec;18(3):667-72. doi: 10.1016/s0888-7543(05)80371-4. Genomics. 1993. PMID: 8307578

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