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Flück, Christa; Deladoey, J.; Rutishauser, K.; Eblé, A.; Marti, U.; Wu, W.; Mullis, P. E. (1998). Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C). Journal of clinical endocrinology and metabolism, 83(10), pp. 3727-3734. Endocrine Society 10.1210/jcem.83.10.5172
Cao, Y.; Wagner, J.K.; Eblé, A.; Hindmarsh, P.; Mullis, P.E. (1994). BamHI RFLP for the GHRHR locus. Human molecular genetics, 3(4), p. 682. Oxford University Press 10.1093/hmg/3.4.682
