Rare Diseases
Records 1 - 3 (of 3 Records) |
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Genetic mutations contributing to non-obstructive azoospermia. Peña Vanessa N et al. Best practice & research. Clinical endocrinology & metabolism 2020 Dec 101479 |
Evaluating co-created patient-facing materials to increase understanding of genetic test results. Dwyer Andrew A et al. Journal of genetic counseling 2020 Oct |
Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism. Kim Ja Hye et al. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2018 Sep |