Hung WY - Search Results

1

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.

Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D, et al. Siddique T, et al. Among authors: hung wy. N Engl J Med. 1991 May 16;324(20):1381-4. doi: 10.1056/NEJM199105163242001. N Engl J Med. 1991. PMID: 2020294 Free article.

2

Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

Pericak-Vance MA, Bebout JL, Gaskell PC Jr, Yamaoka LH, Hung WY, Alberts MJ, Walker AP, Bartlett RJ, Haynes CA, Welsh KA, et al. Pericak-Vance MA, et al. Among authors: hung wy. Am J Hum Genet. 1991 Jun;48(6):1034-50. Am J Hum Genet. 1991. PMID: 2035524 Free PMC article.

3

Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!

Kandt RS, Pericak-Vance MA, Hung WY, Gardner RJ, Crossen PE, Nellist MD, Speer MC, Roses AD. Kandt RS, et al. Among authors: hung wy. Ann N Y Acad Sci. 1991;615:284-97. doi: 10.1111/j.1749-6632.1991.tb37770.x. Ann N Y Acad Sci. 1991. PMID: 2039152

4

Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I.

Vance JM, Pericak-Vance MA, Yamaoka LH, Speer MC, Rosenwasser GO, Small K, Gaskell PC Jr, Hung WY, Alberts MJ, Haynes CS, et al. Vance JM, et al. Among authors: hung wy. Am J Hum Genet. 1989 Jan;44(1):25-9. Am J Hum Genet. 1989. PMID: 2491777 Free PMC article.

5

Absence of linkage of ABO blood group locus to familial tuberous sclerosis.

Kandt RS, Pericak-Vance MA, Hung WY, Gardner RJ, Nellist M, Phillips K, Warner K, Speer MC, Crossen PE, Laing NG, et al. Kandt RS, et al. Among authors: hung wy. Exp Neurol. 1989 Jun;104(3):223-8. doi: 10.1016/0014-4886(89)90033-2. Exp Neurol. 1989. PMID: 2721625

6

Linkage analysis in familial amyotrophic lateral sclerosis.

Siddique T, Pericak-Vance MA, Brooks BR, Roos RP, Hung WY, Antel JP, Munsat TL, Phillips K, Warner K, Speer M, et al. Siddique T, et al. Among authors: hung wy. Neurology. 1989 Jul;39(7):919-25. doi: 10.1212/wnl.39.7.919. Neurology. 1989. PMID: 2739919

7

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.

Hentati A, Ouahchi K, Pericak-Vance MA, Nijhawan D, Ahmad A, Yang Y, Rimmler J, Hung W, Schlotter B, Ahmed A, Ben Hamida M, Hentati F, Siddique T. Hentati A, et al. Neurogenetics. 1998 Dec;2(1):55-60. doi: 10.1007/s100480050052. Neurogenetics. 1998. PMID: 9933301

8

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Among authors: hung wy. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

9

Genetic linkage analysis of nerve growth factor (beta) in familial Alzheimer's disease.

Alberts MJ, Pericak-Vance MA, Royal V, Bebout J, Gaskell P, Thomas J, Hung WY, Clark C, Earl N, Roses AD. Alberts MJ, et al. Among authors: hung wy. Ann Neurol. 1991 Aug;30(2):216-9. doi: 10.1002/ana.410300217. Ann Neurol. 1991. PMID: 1680304

10

MspI RFLP for microtubule associated protein-2 (MAP2).

Alberts MJ, Kandt RS, Pericak-Vance MA, Bebout J, Speer MC, Siddique TS, Yamaoka L, Hung WY, Gaskell PC, Roses AD. Alberts MJ, et al. Among authors: hung wy. Nucleic Acids Res. 1991 Feb 25;19(4):960. doi: 10.1093/nar/19.4.960. Nucleic Acids Res. 1991. PMID: 1708129 Free PMC article.

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