JEFFREY NOEBELS to Craniofacial Abnormalities
This is a "connection" page, showing publications JEFFREY NOEBELS has written about Craniofacial Abnormalities.
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Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Hum Mol Genet. 2007 Aug 01; 16(15):1802-13.
Score: 0.015
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Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome. Epilepsia. 2001 Sep; 42(9):1103-11.
Score: 0.010