Brzustowicz LM - Search Results

1

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3.

Brzustowicz LM, Lehner T, Castilla LH, Penchaszadeh GK, Wilhelmsen KC, Daniels R, Davies KE, Leppert M, Ziter F, Wood D, et al. Brzustowicz LM, et al. Nature. 1990 Apr 5;344(6266):540-1. doi: 10.1038/344540a0. Nature. 1990. PMID: 2320125

2

Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.

Brzustowicz LM, Kleyn PW, Boyce FM, Lien LL, Monaco AP, Penchaszadeh GK, Das K, Wang CH, Munsat TL, Ott J, et al. Brzustowicz LM, et al. Genomics. 1992 Aug;13(4):991-8. doi: 10.1016/0888-7543(92)90012-h. Genomics. 1992. PMID: 1505990

3

Genetic analysis of childhood-onset spinal muscular atrophy.

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

4

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. Among authors: brzustowicz lm. Nature. 1990 Jun 28;345(6278):823-5. doi: 10.1038/345823a0. Nature. 1990. PMID: 1972783

5

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. Am J Hum Genet. 1995 Jan;56(1):210-5. Am J Hum Genet. 1995. PMID: 7825580 Free PMC article.

6

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. Hum Hered. 1993 Nov-Dec;43(6):380-7. doi: 10.1159/000154164. Hum Hered. 1993. PMID: 7904586

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

8

Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.

Brzustowicz LM, Allitto BA, Matseoane D, Theve R, Michaud L, Chatkupt S, Sugarman E, Penchaszadeh GK, Suslak L, Koenigsberger MR, et al. Brzustowicz LM, et al. Am J Hum Genet. 1994 Mar;54(3):482-8. Am J Hum Genet. 1994. PMID: 8116617 Free PMC article.

9

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: brzustowicz lm. Genomics. 1993 Feb;15(2):365-71. doi: 10.1006/geno.1993.1069. Genomics. 1993. PMID: 8449502 Free article.

10

Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus.

Kleyn PW, Brzustowicz LM, Wilhelmsen KC, Freimer NB, Miller JM, Munsat TL, Gilliam TC. Kleyn PW, et al. Among authors: brzustowicz lm. Neurology. 1991 Sep;41(9):1418-22. doi: 10.1212/wnl.41.9.1418. Neurology. 1991. PMID: 1679910

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