Siddique T - 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: siddique t. 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

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. 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.

3

Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.

Isozumi K, DeLong R, Kaplan J, Deng HX, Iqbal Z, Hung WY, Wilhelmsen KC, Hentati A, Pericak-Vance MA, Siddique T. Isozumi K, et al. Among authors: siddique t. Hum Mol Genet. 1996 Sep;5(9):1377-82. doi: 10.1093/hmg/5.9.1377. Hum Mol Genet. 1996. PMID: 8872481

4

Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometry.

Laing NG, Siddique T, Bartlett R, Yamaoka LH, Hung WY, Pericak-Vance MA, Roses AD. Laing NG, et al. Among authors: siddique t. Clin Genet. 1989 Jun;35(6):393-8. doi: 10.1111/j.1399-0004.1989.tb02963.x. Clin Genet. 1989. PMID: 2736788

5

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T. Hentati A, et al. Among authors: siddique t. Hum Mol Genet. 1994 Aug;3(8):1263-7. doi: 10.1093/hmg/3.8.1263. Hum Mol Genet. 1994. PMID: 7987300

6

Linkage analysis in familial amyotrophic lateral sclerosis.

Siddique T, Pericak-Vance MA, Brooks BR, Roos RP, Hung WY, Antel JP, Munsat TL, Phillips K, Warner K, Speer M, et al. Siddique T, et al. Neurology. 1989 Jul;39(7):919-25. doi: 10.1212/wnl.39.7.919. Neurology. 1989. PMID: 2739919

7

Chorea-acanthocytosis: a report of three new families and implications for genetic counselling.

Vance JM, Pericak-Vance MA, Bowman MH, Payne CS, Fredane L, Siddique T, Roses AD, Massey EW. Vance JM, et al. Among authors: siddique t. Am J Med Genet. 1987 Oct;28(2):403-10. doi: 10.1002/ajmg.1320280219. Am J Med Genet. 1987. PMID: 3322006 Review.

8

An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy.

Mérette C, Brzustowicz LM, Daniels RJ, Davies KE, Gilliam TC, Melki J, Munnich A, Pericak-Vance MA, Siddique T, Voosen B, et al. Mérette C, et al. Among authors: siddique t. Genomics. 1994 May 1;21(1):27-33. doi: 10.1006/geno.1994.1220. Genomics. 1994. PMID: 8088801 Free article.

9

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.

Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D, et al. Siddique T, et al. N Engl J Med. 1991 May 16;324(20):1381-4. doi: 10.1056/NEJM199105163242001. N Engl J Med. 1991. PMID: 2020294 Free article.

10

Systematic gene mapping in man: data management considerations.

Pericak-Vance MA, Hung WY, Yamaoka L, Haynes C, Bartlett RJ, Vance JM, Lee J, Siddique T, Gaskell PC, Stajich J, et al. Pericak-Vance MA, et al. Among authors: siddique t. Aust Paediatr J. 1988;24 Suppl 1:87-9. Aust Paediatr J. 1988. PMID: 2904804

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