The technique of H(D) Rydberg atom photofragment translational spectroscopy has been used to investigate the photodissociation dynamics of the mixed isotopomers NH2D and NHD2 following the excitation to the nu’(2) = 0 and 1 levels of their lowest lying (A) over tilde(1)B(1) (C-2 nu) excited electronic states. Peaks in the resulting total kinetic energy release (TKER) spectra are assigned to levels of the NH2, NHD, or ND2 fragments with a wide range of quantum numbers K-a for rotation about their a inertial axes, and with N=K-a, N=K-a+1, or N=K-a+2 as appropriate. These data provide the first measurements of high rotational levels for the ground electronic state of the NHD radical. The least squares fitting of all these spectra, and those resulting from NH3 and ND3, to the best calculated NH2, NHD, and/or ND2 rotational term values provides accurate estimations of the respective N-H and N-D bond dissociation energies D-0(0) the whole series. These values are D-0(0)(H-NH2)=37 115+/-20 cm(-1) (4.602+/-0.002 eV); D-0(0)(H-NHD)=37 240+/-50 cm(-)1; D-0(0)(H-ND2)=37 300+/-30 cm(-1). D-0(0)(D-NHD)=37 880+/-60 cm(-1); and D-0(0)(D-ND2)=38 010+/-20 cm(-1). The differences between these values are fully consistent with differences in zero-point cm energies and lead to a mean value of D-e=40 510+/-25 cm(-1). Dissociation of NH2D or NHD2 through their ((A) over tilde-(X) over tilde 2(0)(1), bands to give an NHD product leads to TKER spectra with a much higher statistical character than those leading to an NH2 or ND2 product, and to those obtained following excitation through the 0(0)(0) bands. This is rationalized in a semiquantitative manner in terms of a varying contribution to the dissociation rate of the parent molecules from internal conversion (IC) to high levels of their respective ground states. Nuclear permutation symmetry appears to play an important role both for the IC rates and for the subsequent branching between product channels.