1. SAPAP Scaffold Proteins: From Synaptic Function to Neuropsychiatric Disorders
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  3. Genotype-dependent epigenetic regulation of DLGAP2 in alcohol use and dependence
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  4. 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature
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  5. Identification and expression pattern of three sex-related genes in the shrimp Neocaridina denticulata sinensis (Decapoda, Caridea)
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  6. 46,XY,r(8)/45,XY,−8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study
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  7. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result
    Chih-Ping Chen et al, 2021, Taiwanese Journal of Obstetrics and Gynecology CrossRef
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  9. 8p23.2p22 deletion: a case report of a large deletion encompassing 8p23.1 with additional clinical features
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  10. Further heterogeneity in Silver–Russell syndrome: PLAG1 deletion in association with a complex chromosomal rearrangement
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  11. Csmd2 Is a Synaptic Transmembrane Protein that Interacts with PSD-95 and Is Required for Neuronal Maturation
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  12. Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region
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  13. Genetic Counseling Challenges: A Case Report of a 6-Year-Old Child with Developmental Delay and B-Acute Lymphoblastic Leukemia
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  14. Partial Trisomy of Chromosome 13 with a Novel Translocation (8 ; 13) and Unique Clinical Presentation in a Palestinian Infant
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  15. Prenatal Diagnosis of 8p23 Deletion Syndrome by Single Nucleotide Polymorphism Microarray
    Didem Kaymak et al, 2021, Journal of Fetal Medicine CrossRef
  16. Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesis
    Chih-Ping Chen et al, 2023, Taiwanese Journal of Obstetrics and Gynecology CrossRef
  17. A novel genotype-phenotype between persistent-cloaca-related VACTERL and mutations of 8p23 and 12q23.1
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