Kleyn PW - Search Results

1

Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region.

Kleyn PW, Wang CH, Lien LL, Vitale E, Pan J, Ross BM, Grunn A, Palmer DA, Warburton D, Brzustowicz LM, et al. Kleyn PW, et al. Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6801-5. doi: 10.1073/pnas.90.14.6801. Proc Natl Acad Sci U S A. 1993. PMID: 8341701 Free PMC article.

2

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. 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.

3

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. Among authors: kleyn pw. Genomics. 1992 Aug;13(4):991-8. doi: 10.1016/0888-7543(92)90012-h. Genomics. 1992. PMID: 1505990

4

Refinement of the spinal muscular atrophy locus by genetic and physical mapping.

Wang CH, Kleyn PW, Vitale E, Ross BM, Lien L, Xu J, Carter TA, Brzustowicz LM, Obici S, Selig S, et al. Wang CH, et al. Among authors: kleyn pw. Am J Hum Genet. 1995 Jan;56(1):202-9. Am J Hum Genet. 1995. PMID: 7825579 Free PMC article.

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

7

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

8

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. Neurology. 1991 Sep;41(9):1418-22. doi: 10.1212/wnl.41.9.1418. Neurology. 1991. PMID: 1679910

9

Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.

Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA. Banerjee P, et al. Among authors: kleyn pw. Genomics. 1998 Mar 1;48(2):171-7. doi: 10.1006/geno.1997.5174. Genomics. 1998. PMID: 9521870 Free article.

10

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

Banerjee P, Kleyn PW, Knowles JA, Lewis CA, Ross BM, Parano E, Kovats SG, Lee JJ, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC. Banerjee P, et al. Among authors: kleyn pw. Nat Genet. 1998 Feb;18(2):177-9. doi: 10.1038/ng0298-177. Nat Genet. 1998. PMID: 9462751

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