An Xp; Yq Translocation Causing a Novel Contiguous Gene Syndrome in Brothers with Generalized Epilepsy, Ichthyosis, and Attention Deficits
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
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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. An updated review on animal models to study attention-deficit hyperactivity disorder;Translational Psychiatry;2024-04-11
3. Characteristics and clinical evaluation of X chromosome translocations;Molecular Cytogenetics;2023-12-21
4. Case report: Sex-specific characteristics of epilepsy phenotypes associated with Xp22.31 deletion: a case report and review;Frontiers in Genetics;2023-06-06
5. Xp;Yq Unbalanced Translocation with Pseudoautosomal Region Aberrations in a Natural Two-Generation Transmission;BioMed Research International;2020-12-04
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