Background publications
|
Ghizzoni, Duquesnoy, Torresani, Vottero, Goossens, Bernasconi: "Isolated growth hormone deficiency type IA associated with a 45-kilobase gene deletion within the human growth hormone gene cluster in an Italian family." in: Pediatric research, Vol. 36, Issue 5, pp. 654-9, 1995 (PubMed).
Duquesnoy, Sobrier, Duriez, Dastot, Buchanan, Savage, Preece, Craescu, Blouquit, Goossens et al.: "A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing ..." in: The EMBO journal, Vol. 13, Issue 6, pp. 1386-95, 1994 (PubMed).
Urbanek, Russell, Cooke, Liebhaber: "Functional characterization of the alternatively spliced, placental human growth hormone receptor." in: The Journal of biological chemistry, Vol. 268, Issue 25, pp. 19025-32, 1993 (PubMed).
|