Willems P - Search Results

1

Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome.

Clayton-Smith J, Webb T, Robb SA, Dijkstra I, Willems P, Lam S, Cheng XJ, Pembrey ME, Malcolm S. Clayton-Smith J, et al. Among authors: willems p. Am J Med Genet. 1992 Sep 15;44(2):256-60. doi: 10.1002/ajmg.1320440236. Am J Med Genet. 1992. PMID: 1360768

2

Recurrence risk in the Angelman ("happy puppet") syndrome.

Willems PJ, Dijkstra I, Brouwer OF, Smit GP. Willems PJ, et al. Am J Med Genet. 1987 Aug;27(4):773-80. doi: 10.1002/ajmg.1320270405. Am J Med Genet. 1987. PMID: 3321989 Review.

3

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.

Buiting K, Dittrich B, Gross S, Lich C, Färber C, Buchholz T, Smith E, Reis A, Bürger J, Nöthen MM, Barth-Witte U, Janssen B, Abeliovich D, Lerer I, van den Ouweland AM, Halley DJ, Schrander-Stumpel C, Smeets H, Meinecke P, Malcolm S, Gardner A, Lalande M, Nicholls RD, Friend K, Schulze A, Matthijs G, Kokkonen H, Hilbert P, Van Maldergem L, Glover G, Carbonell P, Willems P, Gillessen-Kaesbach G, Horsthemke B. Buiting K, et al. Among authors: willems p. Am J Hum Genet. 1998 Jul;63(1):170-80. doi: 10.1086/301935. Am J Hum Genet. 1998. PMID: 9634532 Free PMC article.

4

Molecular study of chromosome 15 in 22 patients with Angelman syndrome.

Beuten J, Mangelschots K, Buntinx I, Coucke P, Brouwer OF, Hennekam RC, Van Broeckhoven C, Willems PJ. Beuten J, et al. Among authors: willems pj. Hum Genet. 1993 Jan;90(5):489-95. doi: 10.1007/BF00217446. Hum Genet. 1993. PMID: 8094063

5

X-linked hydrocephalus.

Willems PJ, Brouwer OF, Dijkstra I, Wilmink J. Willems PJ, et al. Am J Med Genet. 1987 Aug;27(4):921-8. doi: 10.1002/ajmg.1320270419. Am J Med Genet. 1987. PMID: 3425602

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

[Angelman's happy puppet syndrome].

Brouwer OF, Buntinx IM, Willems PJ, Dijkstra I. Brouwer OF, et al. Among authors: willems pj. Tijdschr Kindergeneeskd. 1990 Jun;58(3):89-91. Tijdschr Kindergeneeskd. 1990. PMID: 2375041 Dutch.

8

Activation of fatty acid oxidation in the Silver-Russell syndrome and the Brachmann-de Lange syndrome.

Willems PJ, Dijkstra I, Schierbeek HH, Berger R, Smit GP. Willems PJ, et al. Am J Med Genet. 1988 Aug;30(4):865-73. doi: 10.1002/ajmg.1320300402. Am J Med Genet. 1988. PMID: 3189409

9

Angelman syndrome in an inbred family.

Beuten J, Hennekam RC, Van Roy B, Mangelschots K, Sutcliffe JS, Halley DJ, Hennekam FA, Beaudet AL, Willems PJ. Beuten J, et al. Among authors: willems pj. Hum Genet. 1996 Mar;97(3):294-8. doi: 10.1007/BF02185757. Hum Genet. 1996. PMID: 8786067 Free article.

10

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ. Verhoeven K, et al. Among authors: willems pj. Am J Hum Genet. 1997 May;60(5):1168-73. Am J Hum Genet. 1997. PMID: 9150164 Free PMC article.

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