Paucity of signs in X linked ocular albinism with a 700 kb deletion spanning the OA1 geneTwo families with dyshidrotic ectodermal dysplasia with limbal hair growth and Bitot-like conjunctival anomaliesConclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1A gene for X-linked optic atrophy is closely linked to Xp11.4-Xp11.2 region of the X-chromosome
author
type
label
N.T. Tijmes