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Human Pathology|July 1, 1996
Complete hydatidiform mole with a coexistent embryoR N Baergen, T Kelly, M J McGinniss, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 20, 2013
Identification of HRAS mutations and absence of GNAQ or GNA11 mutations in deep penetrating neviRyan P Bender, Matthew J McGinniss, Paula Esmay, et al.American Journal of Medical Genetics|January 24, 1998
Prader-Willi and Angelman syndromes: diagnosis with a bisulfite-treated methylation-specific PCR methodK Kosaki, M J McGinniss, A N Veraksa, et al.Genomics|October 1, 1990
Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2G R Cutting, M J McGinniss, L M Kasch, et al.American Journal of Medical Genetics|May 2, 1997
Ring chromosome X in a child with manifestations of Kabuki syndromeM J McGinniss, D H Brown, L W Burke, et al.Genomics|February 1, 1993
Spectrum of mutations in CRM-positive and CRM-reduced hemophilia AM J McGinniss, H H Kazazian, L W Hoyer, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2004
Molecular screening for diseases frequent in Ashkenazi Jews: lessons learned from more than 100,000 tests performed in a commercial laboratoryCharles M Strom, Beryl Crossley, Joy B Redman, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 16, 2002
Eight novel mutations in the HEXA geneMatthew J McGinniss, David H Brown, Andrea Fulwiler, et al.The Journal of Molecular Diagnostics : JMD|August 11, 2007
Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator geneFeras M Hantash, Joy B Redman, Dana Goos, et al.Mutagenesis|March 1, 1987
Refinement of a T-lymphocyte cloning assay to quantify the in vivo thioguanine-resistant mutant frequency in humansJ P O'Neill, M J McGinniss, J K Berman, et al.Pageof 4