Schizophrenia in an adult with 6p25 deletion syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference18 articles.
1. Chromosomal abnormalities and schizophrenia
2. Genetic Insights Into the Neurodevelopmental Hypothesis of Schizophrenia
3. Clinical features of 78 adults with 22q11 deletion syndrome
4. Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen
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2. Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome;Frontiers in Genetics;2023-06-23
3. Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features;American Journal of Medical Genetics Part A;2023-03-20
4. Novel Phenotype of 6p25 Deletion Syndrome Presenting Juvenile Parkinsonism and Brain Calcification;Movement Disorders;2020-05-05
5. A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation;Ophthalmic Genetics;2020-03-03
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