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Prenatal Diagnosis|September 5, 2002
Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screeningMichael D Graf, Prabhcharan Gill, Michael Krew, et al.Clinics in Laboratory Medicine|November 29, 2011
Clinical utility of single nucleotide polymorphism arraysStuart SchwartzCurrent Protocols in Human Genetics|April 2, 2015
Preparation of Amniocytes for Interphase Fluorescence In Situ Hybridization (FISH)Stuart SchwartzGround Water|July 9, 2016
Automating Recession Curve Displacement Recharge EstimationBrennan Smith, Stuart SchwartzMedicine and Health, Rhode Island|December 17, 2009
Diagnosis and management of acute goutNazli Conway, Stuart SchwartzGenes|February 27, 2026
Prenatal Microarray Analysis of Pregnancies Without Ultrasound Anomalies: Establishment of Copy Number and Homozygosity Frequencies in Low-Risk PopulationStuart Schwartz, Robert G BestAmerican Journal of Medical Genetics. Part A|April 27, 2004
Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotypeCathy Chu, Stuart Schwartz, Elizabeth McPhersonJournal of Clinical Rheumatology : Practical Reports on Rheumatic & Musculoskeletal Diseases|July 27, 2012
Fatal Henoch-Schönlein purpura in an adult with Dieulafoy lesionsDan A Cristescu, Candice Yuvienco, Stuart SchwartzPersonalized Medicine|May 18, 2018
Genetic testing insurance coverage trends: a review of publicly available policies from the largest US payersMichael D Graf, Denise F Needham, Nicole Teed, et al.American Journal of Medical Genetics. Part A|April 14, 2007
Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndromeMelissa A Dempsey, Stuart Schwartz, Darrel J WaggonerPageof 7