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

• Genetically Confirmed Schwartz–Jampel Syndrome: An Ultra-Rare Case of Congenital Myotonia with Osteochondrodysplasia from India

  Nandita Vivekanand Jali, Suvarna Magar, Tanya Trikha, Varsha Vaidya, Viranchi Vaidya

  S270
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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

• Managing Hyperphagia, Obesity, and Hyperglycemia in Prader-Willi Syndrome: A Meta-Analysis of GLP-1 Agonists and SGLT2 Inhibitors

  Saumika Mulluri

  S209

• 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

• Survival Factors in Lung Cancer Patients with Mutations in the PROS1, SERPINC1, F2, and F5 Genes

  Raniya Ahmad, Ryan Brownlee, Aditya Birla, Dongyu Zhang, Hung Bui, Mashoor Al Ahammed, Girindra Raval

  S217

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

  Abdullah T. Eissa

  127-130