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Boehm,              U, Bouloux,                PM,              Dattani, MT,                de Roux, N,                Dod\u00e9, C,                Dunkel, L,              et al. Expert consensus document: European            Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis            and treatment. Nat Rev Endocrinol          2015;11: 547\u201364.","DOI":"10.1038\/nrendo.2015.112"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Raivio,              T, Avbelj,                M, McCabe,                MJ, Romero,                CJ, Dwyer,                AA,                Tommiska,            J, et al.            Genetic overlap in Kallmann syndrome, combined pituitary hormone            deficiency, and septo-optic dysplasia. J Clin Endocrinol            Metab          2012;97: E694\u20139.","DOI":"10.1210\/jc.2011-2938"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Erba\u015f,              \u0130M, Paket\u00e7i,                A, Acar,                S, Kotan,                LD, Demir,                K, Abac\u0131,                A, et al.            A nonsense variant in <i>FGFR1<\/i>: a rare cause of combined            pituitary hormone deficiency. J Pediatr Endocrinol            Metab          2020;33: 1613\u20135.","DOI":"10.1515\/jpem-2020-0029"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Correa,              FA, Trarbach,                EB, Tusset,                C,                Latronico,              AC,                Montenegro,              LR, Carvalho,                LR, et al.            FGFR1 and PROKR2 rare variants found in patients with combined pituitary            hormone deficiencies. Endocr Connect          2015;4: 100\u20137.","DOI":"10.1530\/EC-15-0015"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Fukami,              M, Iso,                M, Sato,                N,              Igarashi, M,                Seo, M,                Kazukawa,            I, et al.            Submicroscopic deletion involving the fibroblast growth factor receptor 1            gene in a patient with combined pituitary hormone deficiency.            Endocr J          2013;60: 1013\u201320.","DOI":"10.1507\/endocrj.EJ13-0023"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Richards,                S, Aziz,                N, Bale,                S, Bick,                D, Das,                S,                Gastier-Foster,              J, et al.            ACMG Laboratory Quality Assurance Committee.            Standards and guidelines for the interpretation of sequence variants: a            joint consensus recommendation of the American College of Medical Genetics and Genomics            and the Association for Molecular Pathology. Genet Med          2015;17: 405\u201324.","DOI":"10.1038\/gim.2015.30"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Aoyama,              K, Mizuno,                H, Tanaka,                T, Togawa,                T, Negishi,                Y, Ohashi,                K, et al.            Molecular genetic and clinical delineation of 22 patients with congenital            hypogonadotropic hypogonadism. 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