December 1, 2024Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomesAuthorsAlexandra Arreola, Gloria Haskell, Inder Gadi, Andrea Penton, Stuart Schwartz Read more »
March 20, 2025Multiple Deletions In Chromosome 13 Mediated By Chromothripsis: A Case ReportAuthorsZach Ou, MD; Judith Knops, PhD; Deanna Hutchinson, MS; Inder Gadi, PhD; Bing Huang, PhD Read more »
March 20, 2025Understanding prenatal chromosomal abnormalities; importance of both chromosomal and microarray aberrationsAuthorsBob Best, PhD; Alexandra Arreola, PhD; Inder Gadi, PhD; Gloria Haskell, PhD; Bing Huang, PhD; Judith Knops, PhD; Andrea Penton, PhD; Karen Phillips, PhD; James Tepperberg, PhD; Stuart Schwartz, PhD Read more »
March 20, 2025Examination of prenatal cases referred for uniparental disomy 16: Referral patterns, positive associations and key findings AuthorsAndrea Penton, PhD; Alexandra Arreola, PhD; Inder Gadi, PhD; Gloria Haskell, PhD; Karen Phillips, PhD; Amanda Sussman, PhD; James Tepperberg, PhD; Stuart Schwartz, PhD Read more »
March 20, 2025Case report: Incidental Diagnosis of Mulchandani-Bhoj-Conlin Syndrome by Prenatal MicroarrayAuthorLauren Petrarca, MS, GCG Read more »
March 20, 2025Expanding the fetal phenotype of USP7-related conditionsAuthorsLindsey Victoria, MSPH,CGC; Réka Müller, MSPH, LCGC; Nevena Krstić, MS, LCGC Read more »
