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Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report
The idiopathic hypogonadotropic hypogonadism (IHH) is portrayed as missing or fragmented pubescence, cryptorchidism, small penis, and infertility. Clinically it is characterized by the low level of sex steroids and gonadotropins, normal radiographic findings of the hypothalamic-pituitary areas, and...
Autores principales: | Abdullah, Li, Cui, Zhao, Minggang, Wang, Xiang, Li, Xu, Xing, Junping |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100857/ https://www.ncbi.nlm.nih.gov/pubmed/33968667 http://dx.doi.org/10.21037/tau-20-1087 |
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