P624: First case of a FBXW11-related disorder diagnosed via prenatal whole exome sequencing by Lisa Pilchman, Beverly Coleman, Julie Moldenhauer

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P623: Prenatal diagnosis of a RNU4ATAC-related disorder detected by whole genome sequencing not seen by exome sequencing on the initial proband by Lisa Pilchman, Beverly Coleman, Allan Fisher, Natasha Combs, Kendall Kaufmann, Julie Moldenhauer, Juliana Gebb

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P774: Diagnosis of Au Kline syndrome in a fetus with lower urinary tract obstruction: Case report and literature review by Natalie Burrill, Nahla Khalek, Desiree Fiorentino, Beverly Coleman, Erica Schindewolf, Lisa Pilchman, Renee Wright, Haley Crane

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P773: Fetus with Cole-Carpenter type 2 presenting with novel neonatal lethal skeletal dysplasia by Natalie Burrill, Christina Paidas Teefey, Renee Wright, Minh-Huy Le Huynh, Erica Schindewolf, Lisa Pilchman, Haley Crane

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P767: Genetics of prenatally diagnosed micro/anophthalmia by Natalie Burrill, Julie Moldenhauer, Erica Schindewolf, Renee Wright, Lisa Pilchman, Haley Crane, Edward Oliver, Nahla Khalek, Juliana Gebb, Christina Paidas Teefey, Shelly Soni

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P785: Milroy disease presenting as hydrops fetalis: A case series by Haley Crane, Julie Moldenhauer, Nahla Khalek, Juliana Gebb, Christina Paidas Teefey, Erica Schindewolf, Natalie Burrill, Lisa Pilchman, Renee Wright, Alexandra Borst, Michael Fox, Beverly Coleman, Shelly Soni

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P783: Two fetuses with hereditary hemorrhagic telangiectasia presenting with rare finding of arteriovenous malformations by Natalie Burrill, Christina Paidas Teefey, Nankee Kumar, Sonika Agarwal, Lauren Beslow, Edward Oliver, Minh-Huy Le Huynh, Elizabeth Goldmuntz, Bryan Pukenas, Alexandra Borst, Allison Britt, Arastoo Vossough, Stephanie Fuller, Shih-Shan Lang Chen, Erica Schindewolf, Lisa Pilchman, Renee Wright, Haley Crane

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