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Biorxiv : the Preprint Server for Biology|February 19, 2024
Peptide-based capture-and-release purification of extracellular vesicles and statistical algorithm enabled quality assessmentZachary F Greenberg, Samantha Ali, Thomas D Schmittgen, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopiaN Matsumoto, R J Leventer, J A Kuc, et al.
American Journal of Medical Genetics|May 1, 1986
The Perlman familial nephroblastomatosis syndromeF Greenberg, F Stein, M V Gresik, et al.
Human Molecular Genetics|December 15, 2000
The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 geneC Cardoso, R J Leventer, N Matsumoto, et al.
American Journal of Medical Genetics|January 20, 1997
The Pointer syndrome: a new syndrome with skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficultiesA H Huq, R M Braverman, F Greenberg, et al.
Pediatrics|February 1, 1993
Prader-Willi syndrome: consensus diagnostic criteriaV A Holm, S B Cassidy, M G Butler, et al.
ACS Applied Materials & Interfaces|September 12, 2025
RNA Sequencing at Single Vesicle Resolution via 3D Printed Embedded Droplet ArraysAndrew A Brock, Senthilkumar Duraivel, Jinmai Jiang, et al.
Human Molecular Genetics|June 13, 1998
Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombinationW P Robinson, B D Kuchinka, F Bernasconi, et al.
Extracellular Vesicle|July 3, 2024
Understanding molecular characteristics of extracellular vesicles derived from different types of mesenchymal stem cells for therapeutic translationZuo Ding, Zachary F Greenberg, Maria Fernanda Serafim, et al.
American Journal of Obstetrics and Gynecology|February 1, 1984
Clinical interpretation of maternal serum alpha-fetoprotein concentrationsM J Adams, G C Windham, L M James, et al.
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