Gilliam TC - Search Results

1

Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.

Lien LL, Boyce FM, Kleyn P, Brzustowicz LM, Menninger J, Ward DC, Gilliam TC, Kunkel LM. Lien LL, et al. Among authors: gilliam tc. Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7873-6. doi: 10.1073/pnas.88.17.7873. Proc Natl Acad Sci U S A. 1991. PMID: 1881920 Free PMC article.

2

Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.

Selig S, Bruno S, Scharf JM, Wang CH, Vitale E, Gilliam TC, Kunkel LM. Selig S, et al. Among authors: gilliam tc. Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3702-6. doi: 10.1073/pnas.92.9.3702. Proc Natl Acad Sci U S A. 1995. PMID: 7731968 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

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

5

Genetic analysis of childhood-onset spinal muscular atrophy.

Brzustowicz LM, Wilhelmsen KC, Gilliam TC. Brzustowicz LM, et al. Among authors: gilliam tc. Adv Neurol. 1991;56:181-7. Adv Neurol. 1991. PMID: 1853756 No abstract available.

6

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.

7

A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions.

Carter TA, Bönnemann CG, Wang CH, Obici S, Parano E, De Fatima Bonaldo M, Ross BM, Penchaszadeh GK, Mackenzie A, Soares MB, Kunkel LM, Gilliam TC. Carter TA, et al. Among authors: gilliam tc. Hum Mol Genet. 1997 Feb;6(2):229-36. doi: 10.1093/hmg/6.2.229. Hum Mol Genet. 1997. PMID: 9063743

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

9

High resolution physical map of the region surrounding the spinal muscular atrophy gene.

Thompson TG, Morrison KE, Kleyn P, Bengtsson U, Gilliam TC, Davies KE, Wasmuth JJ, McPherson JD. Thompson TG, et al. Among authors: gilliam tc. Hum Mol Genet. 1993 Aug;2(8):1169-76. doi: 10.1093/hmg/2.8.1169. Hum Mol Genet. 1993. PMID: 8401498

10

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

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