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Angelman syndrome: how many genes to remain silent?
Rougeulle C, Lalande M. Rougeulle C, et al. Among authors: lalande m. Neurogenetics. 1998 Aug;1(4):229-37. doi: 10.1007/s100480050034. Neurogenetics. 1998. PMID: 10732796 Review.
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: lalande m. Am J Hum Genet. 1998 Jul;63(1):170-80. doi: 10.1086/301935. Am J Hum Genet. 1998. PMID: 9634532 Free PMC article.
In and around SNRPN.
Lalande M. Lalande M. Nat Genet. 1994 Sep;8(1):5-7. doi: 10.1038/ng0994-5. Nat Genet. 1994. PMID: 7987391 No abstract available.
UBE3A/E6-AP mutations cause Angelman syndrome.
Kishino T, Lalande M, Wagstaff J. Kishino T, et al. Among authors: lalande m. Nat Genet. 1997 Jan;15(1):70-3. doi: 10.1038/ng0197-70. Nat Genet. 1997. PMID: 8988171
209 results