Wang M - Search Results

1

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene.

Collod-Béroud G, Béroud C, Adès L, Black C, Boxer M, Brock DJ, Godfrey M, Hayward C, Karttunen L, Milewicz D, Peltonen L, Richards RI, Wang M, Junien C, Boileau C. Collod-Béroud G, et al. Among authors: wang m. Nucleic Acids Res. 1997 Jan 1;25(1):147-50. doi: 10.1093/nar/25.1.147. Nucleic Acids Res. 1997. PMID: 9016526 Free PMC article.

2

Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome.

Wang M, Kishnani P, Decker-Phillips M, Kahler SG, Chen YT, Godfrey M. Wang M, et al. J Med Genet. 1996 Sep;33(9):760-3. doi: 10.1136/jmg.33.9.760. J Med Genet. 1996. PMID: 8880577 Free PMC article.

3

Familial occurrence of typical and severe lethal congenital contractural arachnodactyly caused by missplicing of exon 34 of fibrillin-2.

Wang M, Clericuzio CL, Godfrey M. Wang M, et al. Am J Hum Genet. 1996 Nov;59(5):1027-34. Am J Hum Genet. 1996. PMID: 8900230 Free PMC article.

4

Prenatal and presymptomatic diagnosis of Marfan syndrome using fluorescence PCR and an automated sequencer.

Wang M, Godfrey M. Wang M, et al. Methods Mol Biol. 1998;92:49-54. doi: 10.1385/0-89603-497-6:49. Methods Mol Biol. 1998. PMID: 9664502 No abstract available.

5

Recurrent mis-splicing of fibrillin exon 32 in two patients with neonatal Marfan syndrome.

Wang M, Price C, Han J, Cisler J, Imaizumi K, Van Thienen MN, DePaepe A, Godfrey M. Wang M, et al. Hum Mol Genet. 1995 Apr;4(4):607-13. doi: 10.1093/hmg/4.4.607. Hum Mol Genet. 1995. PMID: 7633409

6

Prenatal and presymptomatic diagnosis of the Marfan syndrome using fluorescence PCR and an automated sequencer.

Wang M, Mata J, Price CE, Iversen PL, Godfrey M. Wang M, et al. Prenat Diagn. 1995 Jun;15(6):499-507. doi: 10.1002/pd.1970150602. Prenat Diagn. 1995. PMID: 7659684

7

Two novel fibrillin-2 mutations in congenital contractural arachnodactyly.

Belleh S, Zhou G, Wang M, Der Kaloustian VM, Pagon RA, Godfrey M. Belleh S, et al. Among authors: wang m. Am J Med Genet. 2000 May 1;92(1):7-12. Am J Med Genet. 2000. PMID: 10797416

8

Three novel fibrillin mutations in exons 25 and 27: classic versus neonatal Marfan syndrome.

Wang M, Wang JY, Cisler J, Imaizumi K, Burton BK, Jones MC, Lamberti JJ, Godfrey M. Wang M, et al. Among authors: wang jy. Hum Mutat. 1997;9(4):359-62. doi: 10.1002/(SICI)1098-1004(1997)9:4<359::AID-HUMU10>3.0.CO;2-1. Hum Mutat. 1997. PMID: 9101298 No abstract available.

9

Prenatal diagnosis and a donor splice site mutation in fibrillin in a family with Marfan syndrome.

Godfrey M, Vandemark N, Wang M, Velinov M, Wargowski D, Tsipouras P, Han J, Becker J, Robertson W, Droste S, et al. Godfrey M, et al. Among authors: wang m. Am J Hum Genet. 1993 Aug;53(2):472-80. Am J Hum Genet. 1993. PMID: 8101042 Free PMC article.

10

P1148A in fibrillin-1 is not a mutation anymore.

Wang M, Mathews KR, Imaizumi K, Beiraghi S, Blumberg B, Scheuner M, Graham JM Jr, Godfrey M. Wang M, et al. Nat Genet. 1997 Jan;15(1):12. doi: 10.1038/ng0197-12. Nat Genet. 1997. PMID: 8988160 No abstract available.

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