S, V. d. V., E, B., C, B., D, B., M, T., C, H., . . . C, B. (2026). Phenotypic and genotypic analysis of pediatric patients with congenital isolated growth hormone deficiency resulting from biallelic variants in the GHRHR gene: A Belgian registry study. European journal of pediatrics, 185(6), . https://doi.org/10.1007/s00431-026-07039-6
Chicago Style (17th ed.) CitationS, Van de Velde, Boros E, Brunelle C, Beckers D, Thomas M, Heinrichs C, Vlaeminck J, De Schepper J, and Brachet C. "Phenotypic and Genotypic Analysis of Pediatric Patients with Congenital Isolated Growth Hormone Deficiency Resulting from Biallelic Variants in the GHRHR Gene: A Belgian Registry Study." European Journal of Pediatrics 185, no. 6 (2026). https://doi.org/10.1007/s00431-026-07039-6.
MLA (9th ed.) CitationS, Van de Velde, et al. "Phenotypic and Genotypic Analysis of Pediatric Patients with Congenital Isolated Growth Hormone Deficiency Resulting from Biallelic Variants in the GHRHR Gene: A Belgian Registry Study." European Journal of Pediatrics, vol. 185, no. 6, 2026, https://doi.org/10.1007/s00431-026-07039-6.