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Exploring the Genetic Diversity of Isolated Hypogonadotropic Hypogonadism and Its Phenotypic Spectrum: A Case Series
BACKGROUND: Isolated hypogonadotropic hypogonadism (IHH) is a rare disorder being classified as Kallmann syndrome (KS). The present study was conducted to study the genotype and relative proportion of different genetic mutations in IHH and to assess its correlation with phenotype. METHODS: Eleven co...
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| Publicado no: | J Reprod Infertil |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Avicenna Research Institute
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7903671/ https://ncbi.nlm.nih.gov/pubmed/33680884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18502/jri.v22i1.4994 |
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