Inappropriate Feeding Behaviors and Dietary Intakes in Children with FASD or Probable PAE

Por Werts, Rachel L., Van Calcar, Sandra C., Wargowski, David S., Smith, Susan M.
Publicado em 2013

Prenatal diagnosis and a donor splice site mutation in fibrillin in a family with Marfan syndrome

Por Godfrey, Maurice, Vandemark, Natalie, Wang, Mei, Velinov, Milen, Wargowski, David, Tsipouras, Petros, Han, Jenny, Becker, Joanne, Robertson, Wendy, Droste, Sabine, Rao, Velidi H.
Publicado em 1993

Detection of Chromosomal Aberrations by a Whole-Genome Microsatellite Screen

Por Rosenberg, Marjorie J., Vaske, David, Killoran, Christina E., Ning, Yi, Wargowski, David, Hudgins, Louanne, Tifft, Cynthia J., Meck, Jeanne, Blancato, Jan K., Rosenbaum, Kenneth, Pauli, Richard M., Weber, James, Biesecker, Leslie G.
Publicado em 2000

Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology

Por Wilson, Gabrielle R., Sim, Joe C.H., McLean, Catriona, Giannandrea, Maila, Galea, Charles A., Riseley, Jessica R., Stephenson, Sarah E.M., Fitzpatrick, Elizabeth, Haas, Stefan A., Pope, Kate, Hogan, Kirk J., Gregg, Ronald G., Bromhead, Catherine J., Wargowski, David S., Lawrence, Christopher H., James, Paul A., Churchyard, Andrew, Gao, Yujing, Phelan, Dean G., Gillies, Greta, Salce, Nicholas, Stanford, Lynn, Marsh, Ashley P.L., Mignogna, Maria L., Hayflick, Susan J., Leventer, Richard J., Delatycki, Martin B., Mellick, George D., Kalscheuer, Vera M., D’Adamo, Patrizia, Bahlo, Melanie, Amor, David J., Lockhart, Paul J.
Publicado no Am J Hum Genet (2014)