Willems PJ - Search Results

1

BclI RFLP in fucosidase pseudogene (FUCA1P).

Willems PJ, Carritt B, Coucke P, Darby JK, Van der Auwera BJ, O'Brien JS. Willems PJ, et al. Nucleic Acids Res. 1990 Sep 25;18(18):5583. doi: 10.1093/nar/18.18.5583-a. Nucleic Acids Res. 1990. PMID: 1977129 Free PMC article.

2

Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31----q32.

Coucke P, Mangelschots K, Speleman F, Bossuyt P, Van Oostveldt P, Van der Auwera B, Carritt B, Willems PJ. Coucke P, et al. Among authors: willems pj. Cytogenet Cell Genet. 1991;57(2-3):120-2. doi: 10.1159/000133129. Cytogenet Cell Genet. 1991. PMID: 1914520

3

Pvu II RFLP at the human chromosome 1 alpha-L-fucosidase gene locus (FUCA1).

Darby JK, Johnsen J, Nakashima P, Willems PJ, O'Brien JS, Fowler ML, Shows TB, Shooter EM, Cavalli-Sforza LL. Darby JK, et al. Among authors: willems pj. Nucleic Acids Res. 1986 Dec 9;14(23):9543. doi: 10.1093/nar/14.23.9543. Nucleic Acids Res. 1986. PMID: 2879270 Free PMC article. No abstract available.

4

Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patients.

Wauters JG, Hendrickx J, Coucke P, Vits L, Stuer K, van Schil L, van der Auwera BJ, Van Elsen A, Dumon J, Willems PJ, et al. Wauters JG, et al. Among authors: willems pj. Clin Genet. 1991 Feb;39(2):89-92. doi: 10.1111/j.1399-0004.1991.tb02992.x. Clin Genet. 1991. PMID: 1673094

5

Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22.

Willems PJ, Hendrickx J, Van der Auwera BJ, Vits L, Raeymaekers P, Coucke PJ, Van den Bergh I, Berger R, Smit GP, Van Broeckhoven C, et al. Willems PJ, et al. Genomics. 1991 Apr;9(4):565-9. doi: 10.1016/0888-7543(91)90347-h. Genomics. 1991. PMID: 1674721

6

Assignment of X-linked hydrocephalus to Xq28 by linkage analysis.

Willems PJ, Dijkstra I, Van der Auwera BJ, Vits L, Coucke P, Raeymaekers P, Van Broeckhoven C, Consalez GG, Freeman SB, Warren ST, et al. Willems PJ, et al. Genomics. 1990 Oct;8(2):367-70. doi: 10.1016/0888-7543(90)90294-5. Genomics. 1990. PMID: 1979056

7

Restriction analysis of the structural alpha-L-fucosidase gene and its linkage to fucosidosis.

Darby JK, Willems PJ, Nakashima P, Johnsen J, Ferrell RE, Wijsman EM, Gerhard DS, Dracopoli NC, Housman D, Henke J, et al. Darby JK, et al. Among authors: willems pj. Am J Hum Genet. 1988 Nov;43(5):749-55. Am J Hum Genet. 1988. PMID: 2903667 Free PMC article.

8

Fucosidosis revisited: a review of 77 patients.

Willems PJ, Gatti R, Darby JK, Romeo G, Durand P, Dumon JE, O'Brien JS. Willems PJ, et al. Am J Med Genet. 1991 Jan;38(1):111-31. doi: 10.1002/ajmg.1320380125. Am J Med Genet. 1991. PMID: 2012122 Review.

9

Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family.

Willems PJ, Vits L, Wanders RJ, Coucke PJ, Van der Auwera BJ, Van Elsen AF, Raeymaekers P, Van Broeckhoven C, Schutgens RB, Dacremont G, et al. Willems PJ, et al. Arch Neurol. 1990 Jun;47(6):665-9. doi: 10.1001/archneur.1990.00530060077022. Arch Neurol. 1990. PMID: 2161209

10

Two brothers with mental retardation discordant for the fragile-X syndrome.

Van Roy BC, Willems PJ, Vits LJ, Ceulemans BP, Coucke PJ, Van der Auwera BJ, Lormans JA, Dumon JE. Van Roy BC, et al. Among authors: willems pj. Am J Med Genet. 1990 May;36(1):122-5. doi: 10.1002/ajmg.1320360124. Am J Med Genet. 1990. PMID: 2333901

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