[PDF][PDF] Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism
F Gürbüz, LD Kotan, E Mengen, Z Şıklar… - Journal of clinical …, 2012 - jag.journalagent.com
Ob jec ti ve: Normosmic idiopathic hypogonadotropic hypogonadism (nIHH) is characterized
by failure of initiation or maintenance of puberty due to insufficient gonadotropin release,
which is not associated with anosmia/hyposmia. The objective of this study was to determine
the distribution of causative mutations in a hereditary form of nIHH. Methods: In this
prospective collaborative study, 22 families with more than one affected individual (ie
multiplex families) with nIHH were recruited and screened for genes known or suspected to …
by failure of initiation or maintenance of puberty due to insufficient gonadotropin release,
which is not associated with anosmia/hyposmia. The objective of this study was to determine
the distribution of causative mutations in a hereditary form of nIHH. Methods: In this
prospective collaborative study, 22 families with more than one affected individual (ie
multiplex families) with nIHH were recruited and screened for genes known or suspected to …
[PDF][PDF] Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism
LD KOTAN, E Mengen, F GÜRBÜZ, M Berberoglu… - 2012 - openaccess.bezmialem.edu.tr
Objective: Normosmic idiopathic hypogonadotropic hypogonadism (nIHH) is characterized
by failure of initiation or maintenance of puberty due to insufficient gonadotropin release,
which is not associated with anosmia/hyposmia. The objective of this study was to determine
the distribution of causative mutations in a hereditary form of nIHH. Methods: In this
prospective collaborative study, 22 families with more than one affected individual (ie
multiplex families) with nIHH were recruited and screened for genes known or suspected to …
by failure of initiation or maintenance of puberty due to insufficient gonadotropin release,
which is not associated with anosmia/hyposmia. The objective of this study was to determine
the distribution of causative mutations in a hereditary form of nIHH. Methods: In this
prospective collaborative study, 22 families with more than one affected individual (ie
multiplex families) with nIHH were recruited and screened for genes known or suspected to …
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