Concept:
Colour blindness is an X-linked recessive disorder.
Let
\[
X^C=\text{normal vision allele}
\]
\[
X^c=\text{colour blindness allele}
\]
A female is colour blind only when she possesses two recessive alleles.
\[
X^cX^c
\]
Step 1: Write the parental genotypes.
Colour blind woman:
\[
X^cX^c
\]
Normal man:
\[
X^CY
\]
Step 2: Determine the gametes produced.
Female produces:
\[
X^c
\]
Male produces:
\[
X^C,\ Y
\]
Step 3: Construct the offspring genotypes.
Daughters receive:
\[
X^C \text{ from father}
\]
and
\[
X^c \text{ from mother}
\]
Therefore all daughters are
\[
X^CX^c
\]
Step 4: Interpret the phenotype.
Since the dominant normal allele is present,
\[
X^CX^c
\]
shows normal vision.
However, the recessive allele is also present.
Hence daughters are carriers.
\[
\boxed{\text{Normal vision - carrier}}
\]