Wang Q - Search Results

1

Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndrome.

Wang Q, Green E, Barnicoat A, Garrett D, Mullarkey M, Bobrow M, Mathew CG. Wang Q, et al. Lancet. 1993 Oct 23;342(8878):1025-6. doi: 10.1016/0140-6736(93)92882-t. Lancet. 1993. PMID: 8105267 Clinical Trial.

2

A rapid, non-radioactive screening test for fragile X mutations at the FRAXA and FRAXE loci.

Wang Q, Green E, Bobrow M, Mathew CG. Wang Q, et al. J Med Genet. 1995 Mar;32(3):170-3. doi: 10.1136/jmg.32.3.170. J Med Genet. 1995. PMID: 7783163 Free PMC article.

3

Clinical, cytogenetic, and molecular analysis of three families with FRAXE.

Barnicoat AJ, Wang Q, Turk J, Green E, Mathew CG, Flynn G, Buckle V, Hirst M, Davies K, Bobrow M. Barnicoat AJ, et al. Among authors: wang q. J Med Genet. 1997 Jan;34(1):13-7. doi: 10.1136/jmg.34.1.13. J Med Genet. 1997. PMID: 9032643 Free PMC article.

4

The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.

Hirst MC, Barnicoat A, Flynn G, Wang Q, Daker M, Buckle VJ, Davies KE, Bobrow M. Hirst MC, et al. Among authors: wang q. Hum Mol Genet. 1993 Feb;2(2):197-200. doi: 10.1093/hmg/2.2.197. Hum Mol Genet. 1993. PMID: 8499907

5

A variant of Wiskott-Aldrich syndrome with nephropathy is linked to DXS255.

Bennett CP, Barnicoat AJ, Cotter F, Wang Q, Mathew CG. Bennett CP, et al. Among authors: wang q. J Med Genet. 1995 Sep;32(9):757-8. doi: 10.1136/jmg.32.9.757. J Med Genet. 1995. PMID: 8544203 Free PMC article. No abstract available.

6

Combined molecular and cytogenetic analysis for the rapid diagnosis of fragile X syndrome.

Bussani Mastellone C, Giovannucci Uzielli ML, Grasso M, Chiurazzi P, Neri G, Wang Q. Bussani Mastellone C, et al. Among authors: wang q. Acta Genet Med Gemellol (Roma). 1996;45(1-2):165-8. doi: 10.1017/s0001566000001252. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872026

7

Sex-linked deafness.

Petersen MB, Wang Q, Willems PJ. Petersen MB, et al. Among authors: wang q. Clin Genet. 2008 Jan;73(1):14-23. doi: 10.1111/j.1399-0004.2007.00913.x. Epub 2007 Nov 13. Clin Genet. 2008. PMID: 18005182 Review.

8

Mitochondrial DNA control region sequence variation in migraine headache and cyclic vomiting syndrome.

Wang Q, Ito M, Adams K, Li BU, Klopstock T, Maslim A, Higashimoto T, Herzog J, Boles RG. Wang Q, et al. Am J Med Genet A. 2004 Nov 15;131(1):50-8. doi: 10.1002/ajmg.a.30323. Am J Med Genet A. 2004. PMID: 15368478

9

Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation.

van Slegtenhorst M, Verhoef S, Tempelaars A, Bakker L, Wang Q, Wessels M, Bakker R, Nellist M, Lindhout D, Halley D, van den Ouweland A. van Slegtenhorst M, et al. Among authors: wang q. J Med Genet. 1999 Apr;36(4):285-9. J Med Genet. 1999. PMID: 10227394 Free PMC article.

10

Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. Online.

Wang Q, Verhoef S, Tempelaars AM, Bakker PL, Vrtel R, Hesseling-Janssen AL, Nellist M, Oranje AP, Stroink H, Lindhout D, Halley DJ, van den Ouweland AM. Wang Q, et al. Hum Mutat. 1998;11(4):331-2. doi: 10.1002/(SICI)1098-1004(1998)11:4<331::AID-HUMU12>3.0.CO;2-3. Hum Mutat. 1998. PMID: 10215407

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