A daughter inherits two X chromosomes, one from each parent, where a son gets an X and a Y. A father passes his single X to every daughter he has and to none of his sons — and that X is the one he received from his own mother, so a daughter carries a copy of her paternal grandmother's X.
Having two copies leads to something no son experiences. Early in development each of her cells switches one X off at random and every cell descended from it keeps that choice, so she grows up a mosaic: some tissue running her father's X, some her mother's. The clearest illustration is a tortoiseshell cat, whose patches are two coat-colour alleles showing in different cells. In people the effect is subtler, but it is why a carrier of an X-linked trait can sometimes show it mildly or unevenly.
Two X copies also keep recessive X-linked traits hidden. She would need the same variant on both chromosomes to be affected, so
red-green colour vision deficiency reaches roughly 1 in 12 men but only about 1 in 200 women. Daughters are far more often carriers than affected.
Height follows the same mid-parental method used for boys, reversed: subtract about 13 cm (5 inches) from the father's height, average it with the mother's, and most girls finish within roughly 10 cm either side. Her face, meanwhile, is
polygenic — many genes each contributing a little, from both sides.