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Prenatal Diagnosis|July 27, 2010
Is there a correlation between the proportion of cells with isodicentric Yp at amniocentesis and phenotypic sex?Jie Xu, V M SiuAmerican Journal of Medical Genetics|August 3, 2001
Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qterY S Fan, V M SiuAmerican Journal of Medical Genetics|April 15, 1993
18q-mosaicism associated with Rett syndrome phenotypeK Gordon, V M Siu, F Sergovich, et al.Genetic Testing|May 4, 2000
Sensitivity of multiple color spectral karyotyping in detecting small interchromosomal rearrangementsY S Fan, V M Siu, J H Jung, et al.Journal of Autism and Developmental Disorders|July 14, 2001
Brief report: A case of autism with interstitial deletion of chromosome 13M M Steele, M Al-Adeimi, V M Siu, et al.American Journal of Medical Genetics|December 18, 2001
Adrenal insufficiency and hypertension in a newborn infant with Smith-Lemli-Opitz syndromeM J Nowaczyk, V M Siu, P A Krakowiak, et al.Neuropathology and Applied Neurobiology|April 5, 2020
Differential brain region-specific expression of MeCP2 and BDNF in Rett Syndrome patients: a distinct grey-white matter variationS Pejhan, V M Siu, L C Ang, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2001
Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probesY S Fan, Y Zhang, M Speevak, et al.American Journal of Medical Genetics|December 18, 2001
Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical featuresY S Fan, V M Siu, J H Jung, et al.Human Genetics|April 1, 1990
Choroideremia associated with an X-autosomal translocationV M Siu, J R Gonder, J H Jung, et al.Pageof 2