Lunt P - Search Results

1

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.

2

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.

3

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. Among authors: lunt p. Am J Hum Genet. 1992 Aug;51(2):396-403. Am J Hum Genet. 1992. PMID: 1642237 Free PMC article.

4

DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophy.

Lunt PW, Cumming WJ, Kingston H, Read AP, Mountford RC, Mahon M, Harris R. Lunt PW, et al. Lancet. 1989 Jan 7;1(8628):46-7. doi: 10.1016/s0140-6736(89)91704-2. Lancet. 1989. PMID: 2563028 No abstract available.

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

Genetic counselling in facioscapulohumeral muscular dystrophy.

Lunt PW, Harper PS. Lunt PW, et al. J Med Genet. 1991 Oct;28(10):655-64. doi: 10.1136/jmg.28.10.655. J Med Genet. 1991. PMID: 1941962 Free PMC article.

7

Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias.

Lunt PW, Compston DA, Harper PS. Lunt PW, et al. J Med Genet. 1989 Dec;26(12):755-60. doi: 10.1136/jmg.26.12.755. J Med Genet. 1989. PMID: 2614794 Free PMC article.

8

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.

9

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.

10

A workshop on facioscapulohumeral (Landouzy-Déjérine) disease, Manchester, 16 to 17 November 1988.

Lunt PW. Lunt PW. J Med Genet. 1989 Aug;26(8):535-7. doi: 10.1136/jmg.26.8.535. J Med Genet. 1989. PMID: 2671375 Free PMC article. Review. No abstract available.

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