Gilliam TC - Search Results

1

Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy.

Brzustowicz LM, Mérette C, Kleyn PW, Lehner T, Castilla LH, Penchaszadeh GK, Das K, Munsat TL, Ott J, Gilliam TC. Brzustowicz LM, et al. Among authors: gilliam tc. Hum Hered. 1993 Nov-Dec;43(6):380-7. doi: 10.1159/000154164. Hum Hered. 1993. PMID: 7904586

2

Molecular and statistical approaches to the detection and correction of errors in genotype databases.

Brzustowicz LM, Mérette C, Xie X, Townsend L, Gilliam TC, Ott J. Brzustowicz LM, et al. Among authors: gilliam tc. Am J Hum Genet. 1993 Nov;53(5):1137-45. Am J Hum Genet. 1993. PMID: 8213837 Free PMC article.

3

Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B.

Soares VM, Brzustowicz LM, Kleyn PW, Knowles JA, Palmer DA, Asokan S, Penchaszadeh GK, Munsat TL, Gilliam TC. Soares VM, et al. Among authors: gilliam tc. Genomics. 1993 Feb;15(2):365-71. doi: 10.1006/geno.1993.1069. Genomics. 1993. PMID: 8449502 Free article.

4

Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy.

Wang CH, Xu J, Carter TA, Ross BM, Dominski MK, Bellcross CA, Penchaszadeh GK, Munsat TL, Gilliam TC. Wang CH, et al. Among authors: gilliam tc. Hum Mol Genet. 1996 Mar;5(3):359-65. doi: 10.1093/hmg/5.3.359. Hum Mol Genet. 1996. PMID: 8852661

5

Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues.

Wang CH, Carter TA, Das K, Xu J, Ross BM, Penchaszadeh GK, Gilliam TC. Wang CH, et al. Among authors: gilliam tc. Ann Neurol. 1997 Jul;42(1):41-9. doi: 10.1002/ana.410420109. Ann Neurol. 1997. PMID: 9225684

6

No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees.

Knowles JA, Rao PA, Cox-Matise T, Loth JE, de Jesus GM, Levine L, Das K, Penchaszadeh GK, Alexander JR, Lerer B, Endicott J, Ott J, Gilliam TC, Baron M. Knowles JA, et al. Among authors: gilliam tc. Am J Hum Genet. 1998 Apr;62(4):916-24. doi: 10.1086/301785. Am J Hum Genet. 1998. PMID: 9529343 Free PMC article.

7

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: gilliam tc. Genomics. 1994 May 1;21(1):27-33. doi: 10.1006/geno.1994.1220. Genomics. 1994. PMID: 8088801 Free article.

8

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.

Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, et al. Gilliam TC, et al. Nature. 1990 Jun 28;345(6278):823-5. doi: 10.1038/345823a0. Nature. 1990. PMID: 1972783

9

Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy.

Brzustowicz LM, Wang CH, Matseoane D, Kleyn PW, Vitale E, Das K, Penchaszadeh GK, Munsat TL, Hausmanowa-Petrusewicz I, Gilliam TC. Brzustowicz LM, et al. Among authors: gilliam tc. Am J Hum Genet. 1995 Jan;56(1):210-5. Am J Hum Genet. 1995. PMID: 7825580 Free PMC article.

10

Progress toward cloning of the gene responsible for childhood spinal muscular atrophy.

Kleyn PW, Gilliam TC. Kleyn PW, et al. Among authors: gilliam tc. Semin Neurol. 1993 Sep;13(3):276-82. doi: 10.1055/s-2008-1041135. Semin Neurol. 1993. PMID: 8272599 Review. No abstract available.

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