Chromosome abnormality in Kallmann syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference31 articles.
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1. A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome;Scientific Reports;2023-08-10
2. A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome;2023-03-27
3. Comparative pharmacokinetics of seven bioactive components in normal, sham‐operated, and myocardial ischemia–reperfusion injury rats after oral administration of the Salvia Miltiorrhiza–Moutan Cortex herb pair;Biomedical Chromatography;2020-12-02
4. A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator;The Journal of Clinical Endocrinology & Metabolism;2019-10-19
5. Genetic Diagnosis of Hypogonadotropic Hypogonadism and Kallmann Syndrome;Genetic Diagnosis of Endocrine Disorders;2010
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