Advances in Genetic Diagnosis of Kallmann Syndrome and Genetic Interruption

Kallmann syndrome (KS) is a rare hereditary disease with high phenotypic and genetic heterogeneity. Congenital hypogonadotropic hypogonadism and hyposmia/anosmia are the two major characterized phenotypes of KS. Besides, mirror movements, dental agenesis, digital bone abnormalities, unilateral renal...

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Detalles Bibliográficos
Autores principales: Liu, Yujun, Zhi, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110439/
https://www.ncbi.nlm.nih.gov/pubmed/34231173
http://dx.doi.org/10.1007/s43032-021-00638-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110439/
https://www.ncbi.nlm.nih.gov/pubmed/34231173
http://dx.doi.org/10.1007/s43032-021-00638-8

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