Publications
Filters: Author is Dobyns, W B [Clear All Filters]
X-linked malformations of neuronal migration.,
, Neurology, 1996 Aug, Volume 47, Issue 2, p.331-9, (1996)
Abstract
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.,
, Human molecular genetics, 1997 Apr, Volume 6, Issue 4, p.555-62, (1997)
Abstract
Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia.,
, American journal of human genetics, 1997 Aug, Volume 61, Issue 2, p.379-87, (1997)
Abstract
Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndrome.,
, Neurology, 1997 Oct, Volume 49, Issue 4, p.1042-7, (1997)
Abstract
Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation.,
, Neurology, 1998 Aug, Volume 51, Issue 2, p.499-503, (1998)
Abstract
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.,
, Human molecular genetics, 1998 Aug, Volume 7, Issue 8, p.1327-32, (1998)
Abstract