Sarfarazi M - Search Results

1

The use of flanking markers in prediction for Duchenne muscular dystrophy.

Williams H, Sarfarazi M, Brown C, Thomas N, Harper PS. Williams H, et al. Among authors: sarfarazi m. Arch Dis Child. 1986 Mar;61(3):218-22. doi: 10.1136/adc.61.3.218. Arch Dis Child. 1986. PMID: 3457554 Free PMC article.

2

The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).

Upadhyaya M, Lunt P, Sarfarazi M, Broadhead W, Farnham J, Harper PS. Upadhyaya M, et al. Among authors: sarfarazi m. Am J Hum Genet. 1992 Aug;51(2):404-10. Am J Hum Genet. 1992. PMID: 1642238 Free PMC article.

3

Prenatal diagnosis of Duchenne dystrophy.

Harper PS, Williams H, Thomas N, Sarfarazi M. Harper PS, et al. Among authors: sarfarazi m. Lancet. 1985 Apr 13;1(8433):872. doi: 10.1016/s0140-6736(85)92229-9. Lancet. 1985. PMID: 2858728 No abstract available.

4

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.

5

Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy.

Brown CS, Thomas NS, Sarfarazi M, Davies KE, Kunkel L, Pearson PL, Kingston HM, Shaw DJ, Harper PS. Brown CS, et al. Among authors: sarfarazi m. Hum Genet. 1985;71(1):62-74. doi: 10.1007/BF00295671. Hum Genet. 1985. PMID: 2993158

6

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.

Thomas NS, Williams H, Elsas LJ, Hopkins LC, Sarfarazi M, Harper PS. Thomas NS, et al. Among authors: sarfarazi m. J Med Genet. 1986 Dec;23(6):596-8. doi: 10.1136/jmg.23.6.596. J Med Genet. 1986. PMID: 3100805 Free PMC article.

7

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.

8

Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14.

Lunt PW, Noades JG, Upadhyaya M, Sarfarazi M, Harper PS. Lunt PW, et al. Among authors: sarfarazi m. J Neurol Sci. 1988 Dec;88(1-3):287-92. doi: 10.1016/0022-510x(88)90225-0. J Neurol Sci. 1988. PMID: 3225626

9

Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis.

Kingston HM, Sarfarazi M, Newcombe RG, Willis N, Harper PS. Kingston HM, et al. Among authors: sarfarazi m. Clin Genet. 1985 Apr;27(4):383-91. doi: 10.1111/j.1399-0004.1985.tb02280.x. Clin Genet. 1985. PMID: 3995787

10

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.

Kingston HM, Sarfarazi M, Thomas NS, Harper PS. Kingston HM, et al. Among authors: sarfarazi m. Hum Genet. 1984;67(1):6-17. doi: 10.1007/BF00270551. Hum Genet. 1984. PMID: 6086495

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