Mathew CG - Search Results

1

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: mathew cg. 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.

2

A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM.

Differ AM, Bobrow M, Mathew CG. Differ AM, et al. Among authors: mathew cg. Hum Genet. 1992 Aug;89(6):689. doi: 10.1007/BF00221966. Hum Genet. 1992. PMID: 1355071

3

A MseI polymorphism in exon 48 of the dystrophin gene.

Yau SC, Roberts RG, Bentley DR, Mathew CG, Bobrow M. Yau SC, et al. Among authors: mathew cg. Nucleic Acids Res. 1991 Oct 25;19(20):5803. doi: 10.1093/nar/19.20.5803-a. Nucleic Acids Res. 1991. PMID: 1682892 Free PMC article.

4

A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods.

Abbs S, Yau SC, Clark S, Mathew CG, Bobrow M. Abbs S, et al. Among authors: mathew cg. J Med Genet. 1991 May;28(5):304-11. doi: 10.1136/jmg.28.5.304. J Med Genet. 1991. PMID: 1865467 Free PMC article.

5

Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.

Abbs S, Roberts RG, Mathew CG, Bentley DR, Bobrow M. Abbs S, et al. Among authors: mathew cg. Genomics. 1990 Aug;7(4):602-6. doi: 10.1016/0888-7543(90)90205-9. Genomics. 1990. PMID: 1974880

6

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. Among authors: mathew cg. 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.

7

A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

Rousseau F, Heitz D, Tarleton J, MacPherson J, Malmgren H, Dahl N, Barnicoat A, Mathew C, Mornet E, Tejada I, et al. Rousseau F, et al. Am J Hum Genet. 1994 Aug;55(2):225-37. Am J Hum Genet. 1994. PMID: 8037202 Free PMC article. Clinical Trial.

8

Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.

Yau SC, Roberts RG, Bobrow M, Mathew CG. Yau SC, et al. Among authors: mathew cg. Lancet. 1993 Jan 30;341(8840):273-5. doi: 10.1016/0140-6736(93)92618-4. Lancet. 1993. PMID: 8093919

9

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. Among authors: mathew cg. Lancet. 1993 Oct 23;342(8878):1025-6. doi: 10.1016/0140-6736(93)92882-t. Lancet. 1993. PMID: 8105267 Clinical Trial.

10

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: mathew cg. 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.

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