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European Journal of Medical Genetics|February 15, 2011
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL associationNneamaka B Agochukwu, Daniel E Pineda-Alvarez, Amelia A Keaton, et al.American Journal of Medical Genetics. Part A|November 21, 2012
Clinical geneticists' views of VACTERL/VATER associationBenjamin D Solomon, Kelly A Bear, Virginia Kimonis, et al.Cold Spring Harbor Molecular Case Studies|July 14, 2017
Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathyDale L Bodian, Thierry Vilboux, Suchitra K Hourigan, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|December 18, 2013
Analysis of cardiac anomalies in VACTERL associationBridget K Cunningham, Donald W Hadley, Hwaida Hannoush, et al.Circulation. Genomic and Precision Medicine|January 15, 2021
Exome Sequencing and Congenital Heart Disease in Sub-Saharan AfricaEkanem N Ekure, Adebowale Adeyemo, Hanhan Liu, et al.American Journal of Medical Genetics. Part A|February 26, 2015
Expanding the phenotypic spectrum in EP300-related Rubinstein-Taybi syndromeBenjamin D Solomon, Dale L Bodian, Alina Khromykh, et al.Molecular Genetics & Genomic Medicine|December 18, 2018
Cancer genetics program: Follow-up on clinical genetics and genomic medicine in QatarSalha Bujassoum Al-Bader, Reem Alsulaiman, Hekmet Bugrein, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2021
The 2019 US medical genetics workforce: a focus on clinical geneticsBrittany D Jenkins, Catherine G Fischer, Curt A Polito, et al.Translational Psychiatry|July 15, 2020
Mutations in sphingolipid metabolism genes are associated with ADHDMarcela Henriquez-Henriquez, Maria T Acosta, Ariel F Martinez, et al.European Journal of Human Genetics : EJHG|January 15, 2025
GestaltGAN: synthetic photorealistic portraits of individuals with rare genetic disordersAron Kirchhoff, Alexander Hustinx, Behnam Javanmardi, et al.Pageof 29