[p57.sup.KIP2] mutations associated with loss of IGF2 imprinting in Beckwith-Wiedemann syndrome

Authors :: Weksberg, R.
Li, M.
Fei, Y.L.
Shuman, C.
Chitayat, D.
Atkin, J.
Pauli, R.M.
Squire, J.A
Source :: American Journal of Human Genetics. Oct, 2000, Vol. 67 Issue 4, 392
Publication Year :: 2000

Subjects :: Genetic research -- Analysis
Human genetics -- Research
Beckwith-Wiedemann syndrome -- Genetic aspects
Biological sciences

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