A mouse model for Prader-Willi syndrome imprinting-centre mutations

Simplified mammalian DNA isolation procedure

Peter W. Laird, Alice Zijderveld, Koert Linders et al. · Nucleic Acids Research · 1991 · 1.5K citations · Full text

Dna Sequencing, Molecular Biological Method, Natural Sciences +7

UBE3A/E6-AP mutations cause Angelman syndrome

Tatsuya Kishino, Marc Lalande, Joseph Wagstaff · Nature Genetics · 1997 · 1.3K citations

Mendelian Disorder, Genetic Disorder, Angelman Syndrome +6

Prader-Willi Syndrome: Consensus Diagnostic Criteria

Vanja A. Holm, Suzanne B. Cassidy, Merlin G. Butler et al. · PEDIATRICS · 1993 · 1.3K citations · Full text

Metabolic Disorder, Genetic Epidemiology, Diagnosis +18

Antibodies to small nuclear RNAs complexed with proteins are produced by patients with systemic lupus erythematosus

Michael R. Lerner, Joan A. Steitz · Proceedings of the National Academy of Sciences · 1979 · 1.2K citations · Full text

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 884 citations

Infertility, Genetic Testing, Developmental Biology +8