When an electron is free or in the ground state of an atom, its g-factor is 2, as first shown by Dirac. But when an electron or hole is in a conduction band of a crystal, it can be very different from 2, depending upon the crystalline anisotropy and the direction of the applied magnetic induction B. In fact, it can even be 0! To demonstrate this quantitatively, the Dirac equation is extended for a relativistic electron or hole in an orthorhombically-anisotropic conduction band with effective masses mj for j = 1, 2, 3 with geometric mean mg = (m1m2m3) 1/3 . Its covariance is established with general proper and improper Lorentz transformations. The appropriate Foldy-Wouthuysen transformations are extended to evaluate the non-relativistic Hamiltonian to O(mc 2 ) −4 , where mc 2 is the particle's Einstein rest energy. The results can have extremely important consequences for magnetic measurements of many classes of clean anisotropic semiconductors, metals, and superconductors. For B||êµ, the Zeeman gµ factor is 2mWhile propagating in a two-dimensional (2D) conduction band with m3 ≫ m1, m2, g || << 2, consistent with recent measurements of the temperature T dependence of the parallel upper critical induction B c2,|| (T ) in superconducting monolayer NbSe2 and in twisted bilayer graphene. While a particle is in its conduction band of an atomically thin one-dimensional metallic chain along êµ, g << 2 for all B = ∇ × A directions and vanishingly small for B||êµ. The quantum spin Hall Hamiltonian for 2D metals with m1, where E and p − qA are the planar electric field and gauge-invariant momentum, q = ∓|e| is the particle's charge, σ ⊥ is the Pauli matrix normal to the layer, K = ±µB/(2m || c 2 ), and µB is the Bohr magneton.