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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...
Autores principales: | Danda, Vijay Sheker Reddy, Paidipelly, Srinivas Rao, Verepula, Madhavi, Lodha, Piyush, Thaduri, Krishna Reddy, Konda, Chaitanya, Ruhi, Apsia |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Avicenna Research Institute
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7903671/ https://www.ncbi.nlm.nih.gov/pubmed/33680884 http://dx.doi.org/10.18502/jri.v22i1.4994 |
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