Feature Cover: Light‐Activated Nucleic Acid Amplification Systems Using Photo‐Caged DNA Polymerase or Primers (Advanced Genetics 2/07)

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Light‐Activated Nucleic Acid Amplification Systems Using Photo‐Caged DNA Polymerase or Primers

Subjects: “…Genetics…”
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Locus‐Specific Genetic Associations at the DAOA Gene in Schizophrenia and Bipolar Disorder

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Front Cover: PDMSA: A Web‐Based Tool for Pan‐Cancer Survival Analysis Using DNA Methylation Levels as Biomarkers (Advanced Genetics 2/07)

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Issue Information: (Advanced Genetics 2/07)

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Biomaterial Physical Cues as Gene Regulators for Cellular Agriculture

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A Case of Pallister–Killian Syndrome in a Newborn

Subjects: “…Genetics…”
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A Case of Nonimmune Hydrops Fetalis With a Duct-Dependent Systemic Circulation and a Novel Mutation of Kabuki Syndrome

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A Case Highlighting the Importance of Timely Intervention for a Male With AZFb + c Microdeletion

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Clinical Heterogeneity of a TP53 Variant in a Consanguineous Omani Family: A Case Report Featuring a Homozygous Pathogenic Variant

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Prolonged Survival With Homozygous Deletion of Exon 9 in Perlman Syndrome: A Case Report

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Complete Androgen Insensitivity Syndrome (CAIS) Genetic Counseling: Navigating Germline Mosaicism Concerns

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Camptodactyly and Early-Onset Scoliosis in Snijders Blok–Campeau Syndrome

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Novel MYH11 Splice Site Variant Causing Exon Skipping in a Family With Thoracic Aortic Aneurysms and Dissections

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Novel Generation-Skipping Inheritance Pattern of Marfan Syndrome Due to FBN1 Insertional Translocation: Diagnostic Utility of FISH and Implications for Genetic Counseling

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A Rare Case of Concurrent SNRPB Mutation and 22q11.2 Microduplication in a Child With Cerebro-Costo-Mandibular Syndrome

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Three Unrelated Children With Childhood Apraxia of Speech: Exome Sequencing and Functional Gene Analysis Imply a Role of Laminin-511 in Early Neurodevelopment

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Hereditary Myopathy With Early Respiratory Failure Associated With an Incidental COL4A5 Variant: A Case Report

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First Thai Case of Lethal Desbuquois Dysplasia Type I Caused by Novel Compound Heterozygous CANT1 Mutations: Expanding the Molecular Spectrum

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The Ketogenic Diet in the Neonatal Intensive Care Setting: The Case of a Preterm Newborn With Mitochondrial DNA Depletion Syndrome Type 13 (MTDPS13)

Subjects: “…Genetics…”
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