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To study phenotype‐genotype data of Asian−Indian Kallmann syndrome (KS) from our center and systematically review the studies analyzing multiple congenital hypogonadotropic hypogonadism (CHH) genes in KS cohorts using next‐generation sequencing. Click to show full abstract
To study phenotype‐genotype data of Asian−Indian Kallmann syndrome (KS) from our center and systematically review the studies analyzing multiple congenital hypogonadotropic hypogonadism (CHH) genes in KS cohorts using next‐generation sequencing.
Keywords:
genetic spectrum;
center;
spectrum kallmann;
kallmann syndrome;
kallmann;
syndrome single
Journal Title: Clinical Endocrinology
Year Published: 2022
Link to full text (if available)
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Journal Title: Clinical Endocrinology
Year Published: 2022
Link to full text (if available)
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recommendations!