Sarfarazi M - Search Results

1

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.

Meredith AL, Huson SM, Lunt PW, Sarfarazi M, Harley HG, Brook JD, Shaw DJ, Harper PS. Meredith AL, et al. Among authors: sarfarazi m. Br Med J (Clin Res Ed). 1986 Nov 22;293(6558):1353-6. doi: 10.1136/bmj.293.6558.1353. Br Med J (Clin Res Ed). 1986. PMID: 2878705 Free PMC article.

2

Genetic prediction and family structure in Huntington's chorea.

Harper PS, Sarfarazi M. Harper PS, et al. Among authors: sarfarazi m. Br Med J (Clin Res Ed). 1985 Jun 29;290(6486):1929-31. doi: 10.1136/bmj.290.6486.1929. Br Med J (Clin Res Ed). 1985. PMID: 3159461 Free PMC article.

3

A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

Upadhyaya M, Lunt PW, Sarfarazi M, Broadhead W, Daniels J, Owen M, Harper PS. Upadhyaya M, et al. Among authors: sarfarazi m. J Med Genet. 1991 Oct;28(10):665-71. doi: 10.1136/jmg.28.10.665. J Med Genet. 1991. PMID: 1941963 Free PMC article.

4

Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.

Walsh KV, Harley HG, Brook JD, Rundle SA, Sarfarazi M, Harper PS, Shaw DJ. Walsh KV, et al. Among authors: sarfarazi m. Hum Genet. 1990 Aug;85(3):305-10. doi: 10.1007/BF00206751. Hum Genet. 1990. PMID: 1975560

5

Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.

Harley HG, Walsh KV, Rundle S, Brook JD, Sarfarazi M, Koch MC, Floyd JL, Harper PS, Shaw DJ. Harley HG, et al. Among authors: sarfarazi m. Hum Genet. 1991 May;87(1):73-80. doi: 10.1007/BF01213096. Hum Genet. 1991. PMID: 2037285

6

A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes.

Upadhyaya M, Sarfarazi M, Lunt PW, Broadhead W, Harper PS. Upadhyaya M, et al. Among authors: sarfarazi m. J Med Genet. 1989 Aug;26(8):490-3. doi: 10.1136/jmg.26.8.490. J Med Genet. 1989. PMID: 2570156 Free PMC article.

7

Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.

Shaw DJ, Meredith AL, Sarfarazi M, Harley HG, Huson SM, Brook JD, Bufton L, Litt M, Mohandas T, Harper PS. Shaw DJ, et al. Among authors: sarfarazi m. Hum Genet. 1986 Nov;74(3):262-6. doi: 10.1007/BF00282545. Hum Genet. 1986. PMID: 2877933

8

Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.

Harley HG, Brook JD, Jackson CL, Glaser T, Walsh KV, Sarfarazi M, Kent R, Lager M, Koch M, Harper PS, et al. Harley HG, et al. Among authors: sarfarazi m. Genomics. 1988 Nov;3(4):380-4. doi: 10.1016/0888-7543(88)90131-0. Genomics. 1988. PMID: 2907504

9

Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.

Brown CS, Pearson PL, Thomas NS, Sarfarazi M, Harper PS, Shaw DJ. Brown CS, et al. Among authors: sarfarazi m. J Med Genet. 1985 Jun;22(3):179-81. doi: 10.1136/jmg.22.3.179. J Med Genet. 1985. PMID: 2989525 Free PMC article.

10

Gene mapping and myotonic dystrophy.

Harper PS, Shaw D, Meredith L, Sarfarazi M, Brook D, Huson S. Harper PS, et al. Among authors: sarfarazi m. Prog Clin Biol Res. 1985;177:61-76. Prog Clin Biol Res. 1985. PMID: 2989839 No abstract available.

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