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Published in 2022 at "Clinical Endocrinology"
DOI: 10.1111/cen.14822
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.
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Keywords:
genetic spectrum;
center;
spectrum kallmann;
kallmann syndrome ... See more keywords