Fournier’s Gangrene Diagnosis and Treatment: A Systematic Review

por Lewis, Gregory D, Majeed, Maliha, Olang, Catherine A, Patel, Arjun, Gorantla, Vasavi Rakesh, Davis, Nelson, Gluschitz, Sarah
Publicado 2021

A novel unbalanced translocation between chromosomes 5p and 18q leading to dysmorphology and global developmental delay

por Verdi, Giavanna, Li, Dong, Elsea, Sarah H., Nelson, Beverly, Bhoj, Elizabeth J., Hakonarson, Hakon, Yearwood, Katherine R., Upadhya, Sharmila, Gluschitz, Sarah, Smith, Janice L., Sobering, Andrew K.
Publicado 2022

A novel SYNJ1 homozygous variant causing developmental and epileptic encephalopathy in an Afro‐Caribbean individual

por Maj, Mary, Taylor, Christie L., Landau, Kevin, Toriello, Helga V., Li, Dong, Bhoj, Elizabeth J., Hakonarson, Hakon, Nelson, Beverly, Gluschitz, Sarah, Walker, Ruth H., Sobering, Andrew K.
Publicado 2022