Hung WY - Search Results

1

Update on the molecular genetics of Duchenne muscular dystrophy.

Siddique T, Bartlett R, Pericak-Vance M, Yamaoka L, Koh J, Chen J, Hung WY, Kandt R, Roses AD. Siddique T, et al. Among authors: hung wy. Aust Paediatr J. 1988;24 Suppl 1:9-14. Aust Paediatr J. 1988. PMID: 3060079 Review.

2

Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometry.

Laing NG, Siddique T, Bartlett R, Yamaoka LH, Hung WY, Pericak-Vance MA, Roses AD. Laing NG, et al. Among authors: hung wy. Clin Genet. 1989 Jun;35(6):393-8. doi: 10.1111/j.1399-0004.1989.tb02963.x. Clin Genet. 1989. PMID: 2736788

3

RFLP for Duchenne muscular dystrophy cDNA clone 44-1.

Laing NG, Siddique T, Bartlett RJ, Yamaoka LH, Chen JC, Walker AP, Hung WY, Roses AD. Laing NG, et al. Among authors: hung wy. Nucleic Acids Res. 1988 Jul 25;16(14B):7209. doi: 10.1093/nar/16.14.7209. Nucleic Acids Res. 1988. PMID: 2900496 Free PMC article.

4

RFLP for Duchenne muscular dystrophy cDNA clone 30-2.

Walker AP, Bartlett RJ, Laing NG, Siddique T, Yamaoka LH, Chen JC, Hung WY, Roses AD. Walker AP, et al. Among authors: hung wy. Nucleic Acids Res. 1988 Sep 26;16(18):9072. doi: 10.1093/nar/16.18.9072. Nucleic Acids Res. 1988. PMID: 2902573 Free PMC article. No abstract available.

5

Systematic gene mapping in man: data management considerations.

Pericak-Vance MA, Hung WY, Yamaoka L, Haynes C, Bartlett RJ, Vance JM, Lee J, Siddique T, Gaskell PC, Stajich J, et al. Pericak-Vance MA, et al. Among authors: hung wy. Aust Paediatr J. 1988;24 Suppl 1:87-9. Aust Paediatr J. 1988. PMID: 2904804

6

Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy.

Speer MC, Pericak-Vance MA, Yamaoka LH, Koh J, Hung WY, Gaskell PC Jr, Vance JM, Bartlett RJ, Roses AD. Speer MC, et al. Among authors: hung wy. Prenat Diagn. 1988 Jul;8(6):427-37. doi: 10.1002/pd.1970080607. Prenat Diagn. 1988. PMID: 3211845

7

Duchenne muscular dystrophy: high frequency of deletions.

Bartlett RJ, Pericak-Vance MA, Koh J, Yamaoka LH, Chen JC, Hung WY, Speer MC, Wapenaar MC, Van Ommen GJ, Bakker E, et al. Bartlett RJ, et al. Among authors: hung wy. Neurology. 1988 Jan;38(1):1-4. doi: 10.1212/wnl.38.1.1. Neurology. 1988. PMID: 3275902

8

An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy.

Sharp NJ, Kornegay JN, Van Camp SD, Herbstreith MH, Secore SL, Kettle S, Hung WY, Constantinou CD, Dykstra MJ, Roses AD, et al. Sharp NJ, et al. Among authors: hung wy. Genomics. 1992 May;13(1):115-21. doi: 10.1016/0888-7543(92)90210-j. Genomics. 1992. PMID: 1577476

9

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

10

Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA.

Samson F, Lee JE, Hung WY, Potter TG, Herbstreith M, Roses AD, Gilbert JR. Samson F, et al. Among authors: hung wy. J Neurosci Res. 1990 Dec;27(4):441-51. doi: 10.1002/jnr.490270403. J Neurosci Res. 1990. PMID: 1706783

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