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...

ανά Neufeld-Kaiser, Whitney A., Cheng, Edith Y., Liu, Yajuan J.
Τόπος έκδοσης BMC Med (2015)

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

ανά Cheng, Andrew, Neufeld-Kaiser, Whitney, Byers, Peter H., Liu, Yajuan J.
Τόπος έκδοσης BMC Cardiovasc Disord (2020)

Genetic consultation

ανά Pagon, Roberta A, Hanson, Nancy B, Neufeld-Kaiser, Whitney, Covington, Maxine L
Έκδοση 2001

Genetic testing

ανά Pagon, Roberta A, Hanson, Nancy B, Neufeld-Kaiser, Whitney, Covington, Maxine L
Έκδοση 2001

Discordant Sex between Fetal Screening & Postnatal Phenotype Requires Evaluation

ανά Byers, Heather M., Neufeld-Kaiser, Whitney, Chang, Edith Y., Tsuchiya, Karen, Oehler, Erin S., Adam, Margaret P.
Τόπος έκδοσης J Perinatol (2018)

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

ανά Deng, Xinxian, Fang, He, Pathak, Asha, Zou, Angela M., Neufeld-Kaiser, Whitney, Malouf, Emily A., Failor, Richard A., Hisama, Fuki M., Liu, Yajuan J.
Τόπος έκδοσης Front Genet (2020)

Copy Number Variant Discrepancy Resolution Using the ClinGen Dosage Sensitivity Map Results in Updated Clinical Interpretations in ClinVar

ανά Riggs, Erin R., Nelson, Tristan, Merz, Andrew, Ackley, Todd, Bunke, Brian, Collins, Christin D., Collinson, Morag N., Fan, Yao-Shan, Goodenberger, McKinsey L., Golden, Denae M., Haglund-Hazy, Linda, Krgovic, Danijela, Lamb, Allen N., Lewis, Zoe, Li, Guang, Liu, Yajuan, Meck, Jeanne, Neufeld-Kaiser, Whitney, Runke, Cassandra K., Sanmann, Jennifer N., Stavropoulos, Dimitri J., Strong, Emma, Su, Meng, Tayeh, Marwan K., Vokac, Nadja Kokalj, Thorland, Erik C., Andersen, Erica, Martin, Christa L.
Τόπος έκδοσης Hum Mutat (2018)