Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary ref...

por Neufeld-Kaiser, Whitney A., Cheng, Edith Y., Liu, Yajuan J.
Publicado 2015

6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotype

por Cheng, Andrew, Neufeld-Kaiser, Whitney, Byers, Peter H., Liu, Yajuan J.
Publicado 2020

Discordant Sex between Fetal Screening & Postnatal Phenotype Requires Evaluation

por Byers, Heather M., Neufeld-Kaiser, Whitney, Chang, Edith Y., Tsuchiya, Karen, Oehler, Erin S., Adam, Margaret P.
Publicado 2018

Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men

por Deng, Xinxian, Fang, He, Pathak, Asha, Zou, Angela M., Neufeld-Kaiser, Whitney, Malouf, Emily A., Failor, Richard A., Hisama, Fuki M., Liu, Yajuan J.
Publicado 2020