DOI:
10.1055/s-00000025
Hormone and Metabolic Research
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References
McCabe MJ, Gaston-Massuet C, Tziaferi V. et al.
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
J Clin Endocrinol Metab 2011;
96: E1709-E1718
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