Genetics

All Items

• Biomedical Engineering Advancements after Management of Myelomeningocele Study (MOMS): A Narrative Review

  Natalie C. Campbell, Stephen B. Trippel, Eric A. Nauman

  405-412

• Comparison of Risk Factors for Developing Liver Fibrosis in Subjects With and Without Metabolic Syndrome: A Cohort Study

  Ana Karen Treviño Morales, Laura Elia Martínez de Villarreal, Geovana Calvo Anguiano, Jesús Zacarías Villarreal Pérez, Sandra Marlen González Peña, Fernando Lavalle González

  S172

• Down Syndrome and Quality of Life: A Case Report

  Hilary L. Schroeder, Marianinha Joanes, Andre Small, Raghu Maramraj,

  112-114

• Exploring the Relationship between Psoriasis and Pregnancy: A Systematic Literature Review

  Pratiksha Patra

  128-133

• Eyelid Tumor and Microcephaly in Hunter's Disease

  Mauricio Alejandro Saldaña-Ruiz, Mauricio Linnery Rendón-Saldívar, Vanessa Pamela Salolin-Vargas, Valeria Monserrat Ramírez-Angulo, Alejandro Garza-Álvarez, Vanessa Jarelly Rodríguez-Huerta

  S406

• Fibroblast Growth Factor (FGF) Receptor Mutations: A Pathway to Understanding Multigenic Risk in Disease?

  Stuart J. Mires

  123-127

• FKBP5 Gene Variants as Predictors for Antidepressant Response in Individuals with Major Depressive Disorder Who Have Experienced Childhood Trauma. A Systematic Review

  Natalie Wietfeldt, Andrew J. Boileau

  126-134
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  HLA-DQB1*0301 in Bullous Pemphigoid and Pemphigus Vulgaris: A Meta-Analysis

  Dylan Thibaut, Ryan Witcher, Breana Barnes, Kersten T. Schroeder

  199-205

• Medical Students Have a Powerful Role in Addressing Community Needs in the COVID-19 Pandemic: An Experience from the US

  Carly O'Connor-Terry, Tejasvi Gowda, Ben Zuchelkowski, Sarah Minney, Jane Kwon

  70-72

• Mutation in Genes FBN1, AKT1, and LMNA: Marfan Syndrome, Proteus Syndrome, and Progeria Share Common Systemic Involvement

  Tonmoy Biswas

  92-101

• Pentalogy of Cantrell: Report Of A Unique Phenotype

  Manuel Vásquez, Wilmar Saldarriaga Gil

  S335

• Prenatal Diagnosis of a Fetus with Partial Duplication and Deletion of Chromosome 18 Due to Maternal Pericentric Inversion 18

  Manuel Alejandro Vásquez Salguero, Wilmar Saldarriaga Gil

  S175

• The Allele Distribution for the rs7250346 SNP in SLC5A5 among Saudis

  Abdullah T. Eissa

  127-130