Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?
Keigo Okamoto, U Friedrich(University of Regensburg), A E Reeve(University of Otago), Niels Tommerup(University of Copenhagen), Ian M. Morison(Dunedin Public Hospital), H. ‐R. Wiedemann(Kiel University)
Cited by 21
Related Papers
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
|Nature|1993|709
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.
|PubMed|1989|308
Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation
|The American Journal of Human Genetics|2003|297
Recurrent Reciprocal Genomic Rearrangements of 17q12 Are Associated with Renal Disease, Diabetes, and Epilepsy
|The American Journal of Human Genetics|2007|268
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.
|Molecular and Cellular Biology|1989|205