Wang CH - Search Results

1

Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy.

Brzustowicz LM, Wang CH, Matseoane D, Kleyn PW, Vitale E, Das K, Penchaszadeh GK, Munsat TL, Hausmanowa-Petrusewicz I, Gilliam TC. Brzustowicz LM, et al. Among authors: wang ch. Am J Hum Genet. 1995 Jan;56(1):210-5. Am J Hum Genet. 1995. PMID: 7825580 Free PMC article.

2

Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.

Brzustowicz LM, Kleyn PW, Boyce FM, Lien LL, Monaco AP, Penchaszadeh GK, Das K, Wang CH, Munsat TL, Ott J, et al. Brzustowicz LM, et al. Among authors: wang ch. Genomics. 1992 Aug;13(4):991-8. doi: 10.1016/0888-7543(92)90012-h. Genomics. 1992. PMID: 1505990

3

Refinement of the spinal muscular atrophy locus by genetic and physical mapping.

Wang CH, Kleyn PW, Vitale E, Ross BM, Lien L, Xu J, Carter TA, Brzustowicz LM, Obici S, Selig S, et al. Wang CH, et al. Am J Hum Genet. 1995 Jan;56(1):202-9. Am J Hum Genet. 1995. PMID: 7825579 Free PMC article.

4

Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region.

Kleyn PW, Wang CH, Lien LL, Vitale E, Pan J, Ross BM, Grunn A, Palmer DA, Warburton D, Brzustowicz LM, et al. Kleyn PW, et al. Among authors: wang ch. Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6801-5. doi: 10.1073/pnas.90.14.6801. Proc Natl Acad Sci U S A. 1993. PMID: 8341701 Free PMC article.

5

Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.

Wang CH, Xu J, Carter TA, Ross BM, Dominski MK, Bellcross CA, Penchaszadeh GK, Munsat TL, Gilliam TC. Wang CH, et al. Hum Mol Genet. 1996 Mar;5(3):359-65. doi: 10.1093/hmg/5.3.359. Hum Mol Genet. 1996. PMID: 8852661

6

A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions.

Carter TA, Bönnemann CG, Wang CH, Obici S, Parano E, De Fatima Bonaldo M, Ross BM, Penchaszadeh GK, Mackenzie A, Soares MB, Kunkel LM, Gilliam TC. Carter TA, et al. Among authors: wang ch. Hum Mol Genet. 1997 Feb;6(2):229-36. doi: 10.1093/hmg/6.2.229. Hum Mol Genet. 1997. PMID: 9063743

7

Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.

Wang CH, Carter TA, Das K, Xu J, Ross BM, Penchaszadeh GK, Gilliam TC. Wang CH, et al. Ann Neurol. 1997 Jul;42(1):41-9. doi: 10.1002/ana.410420109. Ann Neurol. 1997. PMID: 9225684

8

Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.

Selig S, Bruno S, Scharf JM, Wang CH, Vitale E, Gilliam TC, Kunkel LM. Selig S, et al. Among authors: wang ch. Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3702-6. doi: 10.1073/pnas.92.9.3702. Proc Natl Acad Sci U S A. 1995. PMID: 7731968 Free PMC article.

9

Differential SMN2 expression associated with SMA severity.

Gavrilov DK, Shi X, Das K, Gilliam TC, Wang CH. Gavrilov DK, et al. Among authors: wang ch. Nat Genet. 1998 Nov;20(3):230-1. doi: 10.1038/3030. Nat Genet. 1998. PMID: 9806538 No abstract available.

10

Mitochondrial myopathy simulating spinal muscular atrophy.

Pons R, Andreetta F, Wang CH, Vu TH, Bonilla E, DiMauro S, De Vivo DC. Pons R, et al. Among authors: wang ch. Pediatr Neurol. 1996 Sep;15(2):153-8. doi: 10.1016/0887-8994(96)00118-x. Pediatr Neurol. 1996. PMID: 8888051 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,976 results

Search Page

Filters