Syndromic patent ductus arteriosus: Evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder

av Mani, Arya, Radhakrishnan, Jayaram, Farhi, Anita, Carew, Khary S., Warnes, Carole A., Nelson-Williams, Carol, Day, Ronald W., Pober, Barbara, State, Matthew W., Lifton, Richard P.
Publicerad 2005

LRP6 Mutation in a Family with Early Coronary Disease and Metabolic Risk Factors

av Mani, Arya, Radhakrishnan, Jayaram, Wang, He, Mani, Alaleh, Mani, Mohammad-Ali, Nelson-Williams, Carol, Carew, Khary S, Mane, Shrikant, Najmabadi, Hossein, Wu, Dan, Lifton, Richard P.
Publicerad 2007