A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes
δημοσιεύθηκε στο: The Journal of Clinical Endocrinology and Metabolism
date of publication: 2009-12-18
language: Αγγλικά
main subject: Σύνδρομο Κάλμαν
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Article - wd:Q43214533