Lunt P - 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. Among authors: lunt p. 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

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: lunt pw. Hum Mol Genet. 1993 Jul;2(7):981-7. doi: 10.1093/hmg/2.7.981. Hum Mol Genet. 1993. PMID: 8364581

3

Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHD.

Upadhyaya M, Maynard J, Rogers MT, Lunt PW, Jardine P, Ravine D, Harper PS. Upadhyaya M, et al. Among authors: lunt pw. J Med Genet. 1997 Jun;34(6):476-9. doi: 10.1136/jmg.34.6.476. J Med Genet. 1997. PMID: 9192267 Free PMC article.

4

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: lunt pw. 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.

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: lunt pw. 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

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. J Neurol Sci. 1988 Dec;88(1-3):287-92. doi: 10.1016/0022-510x(88)90225-0. J Neurol Sci. 1988. PMID: 3225626

7

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: lunt p. Am J Hum Genet. 1992 Aug;51(2):404-10. Am J Hum Genet. 1992. PMID: 1642238 Free PMC article.

8

Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.

Siddique T, Roper H, Pericak-Vance MA, Shaw J, Warner KL, Hung WY, Phillips KL, Lunt P, Cumming WJ, Roses AD. Siddique T, et al. Among authors: lunt p. J Med Genet. 1989 Aug;26(8):487-9. doi: 10.1136/jmg.26.8.487. J Med Genet. 1989. PMID: 2570155 Free PMC article.

9

Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD).

Lunt PW, Jardine PE, Koch MC, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M. Lunt PW, et al. Hum Mol Genet. 1995 May;4(5):951-8. doi: 10.1093/hmg/4.5.951. Hum Mol Genet. 1995. PMID: 7633457

10

Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy.

Lunt PW, Jardine PE, Koch M, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M. Lunt PW, et al. Muscle Nerve Suppl. 1995;2:S103-9. Muscle Nerve Suppl. 1995. PMID: 7739619

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