Syndromic and Systemic Diagnoses Associated With Isolated Sagittal Synostosis

por Davis, Amani A., Haredy, Mostafa M., Huey, Jennifer, Scanga, Hannah, Zuccoli, Giulio, Pollack, Ian F., Tamber, Mandeep S., Goldstein, Jesse, Madan-Khetarpal, Suneeta, Nischal, Ken K.
Publicado 2019

Diagnostic yield of genetic screening in a diverse, community-ascertained cohort

por Rao, Nandana D., Kaganovsky, Jailanie, Malouf, Emily A., Coe, Sandy, Huey, Jennifer, Tsinajinne, Darwin, Hassan, Sajida, King, Kristine M., Fullerton, Stephanie M., Chen, Annie T., Shirts, Brian H.
Publicado 2023

Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4

por van der Ende, Sarah R., Meyers, Benjamin S., Capasso, Jenina E., Sasongko, Mario, Yonekawa, Yoshihiro, Pihlblad, Matthew, Huey, Jennifer, Bedoukian, Emma C., Krantz, Ian D., Ngo, Michael H., McMaster, Christopher R., Levin, Alex V., Robitaille, Johane M.
Publicado 2022

Extended Family Outreach in Hereditary Cancer Using Web-Based Genealogy, Direct-to-Consumer Ancestry Genetics, and Social Media: Mixed Methods Process Evaluation of the ConnectMyVa...

por Chen, Annie T, Huey, Jennifer, Coe, Sandra, Kaganovsky, Jailanie, Malouf, Emily A, Evans, Heather D, Daker, Jill, Harper, Elizabeth, Fordiani, Olivia, Lowe, Emma E, Oldroyd, Caileigh McGraw, Price, Ashlyn, Roth, Kristlynn, Stoddard, Julie, Crandell, Jill N, Shirts, Brian H
Publicado 2023