Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genes
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference28 articles.
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1. Chromosome Xp22.3 deletion syndrome with X-linked ichthyosis, Kallmann syndrome, short stature, generalized epilepsy, hearing loss, attention deficit hyperactivity disorder, and intellectual disability – A rare report with review of literature;Journal of Neurosciences in Rural Practice;2024-07-13
2. Case report: Sex-specific characteristics of epilepsy phenotypes associated with Xp22.31 deletion: a case report and review;Frontiers in Genetics;2023-06-06
3. X‐linked ichthyosis: New insights into a multi‐system disorder;Skin Health and Disease;2022-10-17
4. Prevalence and Phenotypic Effects of Copy Number Variants in Isolated Hypogonadotropic Hypogonadism;The Journal of Clinical Endocrinology & Metabolism;2022-05-16
5. Novel Microdeletion in the X Chromosome Leads to Kallmann Syndrome, Ichthyosis, Obesity, and Strabismus;Frontiers in Genetics;2020-06-24
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