β Scribed by Wright, Tracy J.; Altherr, Michael R.; Callen, David; Hirschhorn, Kurt
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Wolf-Hirschhorn syndrome (WHS), a multiple congenital malformation syndrome, and Pitt-Rogers-Danks syndrome (PRDS), a rare condition with similar anomalies, were previously thought to be clinically distinct conditions. While WHS has long been associated with deletions near the terminus of 4p, severa
prompted us to re-examine the issue of mosaicism in several cases of atypical Prader-Willi syndrome reported in 1996 [Mowery