Association of hypocalcemia with congenital heart disease in 22q11.2 deletion syndrome

Por Rayannavar, Arpana, Katz, Lorraine E. Levitt, Crowley, Terrence Blaine, Lessig, Megan, Grand, Katheryn, Goldmuntz, Elizabeth, Zackai, Elaine H., McDonald-McGinn, Donna M.
Publicado no Am J Med Genet A (2018)

Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome

Por Schindewolf, Erica, Khalek, Nahla, Johnson, Mark P., Gebb, Juliana, Coleman, Beverly, Crowley, Terrence Blaine, Zackai, Elaine H., McDonald-McGinn, Donna M., Moldenhauer, Julie S.
Publicado no Am J Med Genet A (2018)

Pediatric healthcare costs for patients with 22q11.2 deletion syndrome

Por Benn, Peter, Iyengar, Sushma, Crowley, Terrence Blaine, Zackai, Elaine H., Burrows, Evanette K., Moshkevich, Solomon, McDonald‐McGinn, Donna M., Sullivan, Kathleen E., Demko, Zachary
Publicado no Mol Genet Genomic Med (2017)

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers

Por Unolt, Marta, Versacci, Paolo, Anaclerio, Silvia, Lambiase, Caterina, Calcagni, Giulio, Trezzi, Matteo, Carotti, Adriano, Crowley, Terrence Blaine, Zackai, Elaine H., Goldmuntz, Elizabeth, Gaynor, James William, Digilio, Maria Cristina, McDonald-McGinn, Donna M., Marino, Bruno
Publicado no Am J Med Genet A (2018)