Disruption of the mouse necdin gene results in early post-natal lethality

Prader-Willi Syndrome: Consensus Diagnostic Criteria

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

Medicine, Molecular Genetics, Pediatrics +11

Cre-mediated gene deletion in the mammary gland

Kay‐Uwe Wagner, R.J. Wall, Luc St‐Onge et al. · Nucleic Acids Research · 1997 · 529 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Tao Yang, Todd E. Adamson, James L. Resnick et al. · Nature Genetics · 1998 · 302 citations

Life Sciences, Genetics, Molecular Genetics +11

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region

Tayfun Özçelık, Stuart E. Leff, Wendy P. Robinson et al. · Nature Genetics · 1992 · 296 citations

Life Sciences, Genetics, Molecular Genetics +11

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Philippe Jay, Claire Rougeulle, Annick Massacrier et al. · Nature Genetics · 1997 · 245 citations

Life Sciences, Genetics, Molecular Genetics +9