Sarfarazi M - Search Results

1

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Sarfarazi M, Upadhyaya M, Padberg G, Pericak-Vance M, Siddique T, Lucotte G, Lunt P. Sarfarazi M, et al. J Med Genet. 1989 Aug;26(8):481-4. doi: 10.1136/jmg.26.8.481. J Med Genet. 1989. PMID: 2769720 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

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

Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.

Roberts SH, Upadhyaya M, Sarfarazi M, Harper PS. Roberts SH, et al. Among authors: sarfarazi m. J Med Genet. 1989 May;26(5):309-13. doi: 10.1136/jmg.26.5.309. J Med Genet. 1989. PMID: 2499679 Free PMC article.

5

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.

6

Further exclusion data for the Von Recklinghausen neurofibromatosis gene: a genetic linkage study of 19 polymorphic markers.

Upadhyaya M, Sarfarazi M, Huson SM, Harper PS. Upadhyaya M, et al. Among authors: sarfarazi m. J Med Genet. 1987 Sep;24(9):534-6. doi: 10.1136/jmg.24.9.534. J Med Genet. 1987. PMID: 3118035 Free PMC article.

7

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

8

Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements.

Upadhyaya M, Jardine P, Maynard J, Farnham J, Sarfarazi M, Wijmenga C, Hewitt JE, Frants R, Harper PS, Lunt PW. Upadhyaya M, et al. Among authors: sarfarazi m. Hum Mol Genet. 1993 Jul;2(7):981-7. doi: 10.1093/hmg/2.7.981. Hum Mol Genet. 1993. PMID: 8364581

9

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.

Sarfarazi M, Wijmenga C, Upadhyaya M, Weiffenbach B, Hyser C, Mathews K, Murray J, Gilbert J, Pericak-Vance M, Lunt P, et al. Sarfarazi M, et al. Am J Hum Genet. 1992 Aug;51(2):396-403. Am J Hum Genet. 1992. PMID: 1642237 Free PMC article.

10

Watson syndrome: is it a subtype of type 1 neurofibromatosis?

Allanson JE, Upadhyaya M, Watson GH, Partington M, MacKenzie A, Lahey D, MacLeod H, Sarfarazi M, Broadhead W, Harper PS, et al. Allanson JE, et al. Among authors: sarfarazi m. J Med Genet. 1991 Nov;28(11):752-6. doi: 10.1136/jmg.28.11.752. J Med Genet. 1991. PMID: 1770531 Free PMC article.

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