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Case Reports in Genetics : Impact Factor & More

eISSN: 2090-6552pISSN: 2090-6544
JournalOpen Access
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Case Reports in Genetics Journal Specifications

Overview
Publisher Hindawi Limited
Language English
Article Processing ChargesUSD 725
Publication Time13
Editorial Review ProcessAnonymous peer review
General Details
LanguageEnglish
Website URLVisit website
Publication Details
Other chargesVisit website
PlagiarismVisit website
Publication Time 13
Waiver PolicyVisit website
Editorial Review Detail
Editorial TeamVisit website
Review ProcessAnonymous peer review
Review UrlVisit website
Information for authors
Author instructionsVisit website
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Deposit PolicySherpa/Romeo
License typeCC BY
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Recently Published Papers in Case Reports in Genetics

A Case of Malan Syndrome With Pulmonary Artery Dilatation due to a Novel Frameshift Variant in Exon 2 of the NFIX Gene
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A Case of Pallister\u2013Killian Syndrome in a Newborn
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A Case of Nonimmune Hydrops Fetalis With a Duct\u2010Dependent 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\u2009+\u2009c Microdeletion
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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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The Ketogenic Diet in the Neonatal Intensive Care Setting: The Case of a Preterm Newborn With Mitochondrial DNA Depletion Syndrome Type 13 (MTDPS13)
  • 2 Feb 2026
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A Case of Malan Syndrome With Pulmonary Artery Dilatation due to a Novel Frameshift Variant in Exon 2 of the NFIX Gene
  • 16 Jun 2026
  • Case Reports in Genetics
A Case of Pallister\u2013Killian Syndrome in a Newborn
  • 30 May 2026
  • Case Reports in Genetics
A Case of Nonimmune Hydrops Fetalis With a Duct\u2010Dependent Systemic Circulation and a Novel Mutation of Kabuki Syndrome
  • 29 May 2026
  • Case Reports in Genetics
A Case Highlighting the Importance of Timely Intervention for a Male With AZFb\u2009+\u2009c Microdeletion
  • 21 May 2026
  • Case Reports in Genetics
Novel Generation‐Skipping Inheritance Pattern of Marfan Syndrome Due to FBN1 Insertional Translocation: Diagnostic Utility of FISH and Implications for Genetic Counseling
  • 9 Mar 2026
  • Case Reports in Genetics
The Ketogenic Diet in the Neonatal Intensive Care Setting: The Case of a Preterm Newborn With Mitochondrial DNA Depletion Syndrome Type 13 (MTDPS13)
  • 2 Feb 2026
  • Case Reports in Genetics

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