Mark J. McCabe, et.al., Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction., The Journal of clinical endocrinology and metabolism, 2011, 96
Mark J. McCabe, et.al., Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction., The Journal of clinical endocrinology and metabolism, 2011, 96