Published in Am J Hum Genet on December 01, 1997
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J Med Genet (2008) 3.87
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Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes. Am J Hum Genet (1994) 1.79
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Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion. Clin Genet (1984) 1.06
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndrome. Hum Genet (1992) 0.97
Duplication of proximal 15q as a cause of Prader-Willi syndrome. Am J Med Genet (1987) 0.97
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Form of 15q proximal duplication appears to be a normal euchromatic variant. Am J Med Genet (1994) 0.88
Absence of predictable phenotypic expression in proximal 15q duplications. Clin Genet (1991) 0.86
Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13. J Med Genet (1992) 0.81
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Xp deletions associated with autism in three females. Hum Genet (1999) 2.40
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