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F Greenberg

Showing results (131-140 of 173) with videos related to

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American Journal of Medical Genetics|September 1, 1988
Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomalyF Greenberg, K B Courtney, R A Wessels, et al.
American Journal of Medical Genetics|May 1, 1986
The Perlman familial nephroblastomatosis syndromeF Greenberg, F Stein, M V Gresik, et al.
Progress in Clinical and Biological Research|January 1, 1993
Gene dosage as a mechanism for a common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, C A Wise, 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.
Angewandte Chemie (International Ed. in English)|September 18, 2007
Fluorous-based small-molecule microarrays for the discovery of histone deacetylase inhibitorsArturo J Vegas, James E Bradner, Weiping Tang, 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 Diseases of Children (1960)|February 1, 1988
X-linked infantile spinal muscular atrophyF Greenberg, K R Fenolio, J F Hejtmancik, 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.
Pageof 18

Showing results (131-140 of 173) with videos related to

Sort By:
Pageof 18
American Journal of Medical Genetics|September 1, 1988
Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomalyF Greenberg, K B Courtney, R A Wessels, et al.
American Journal of Medical Genetics|May 1, 1986
The Perlman familial nephroblastomatosis syndromeF Greenberg, F Stein, M V Gresik, et al.
Progress in Clinical and Biological Research|January 1, 1993
Gene dosage as a mechanism for a common autosomal dominant peripheral neuropathy: Charcot-Marie-Tooth disease type 1AB B Roa, C A Garcia, C A Wise, 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.
Angewandte Chemie (International Ed. in English)|September 18, 2007
Fluorous-based small-molecule microarrays for the discovery of histone deacetylase inhibitorsArturo J Vegas, James E Bradner, Weiping Tang, 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 Diseases of Children (1960)|February 1, 1988
X-linked infantile spinal muscular atrophyF Greenberg, K R Fenolio, J F Hejtmancik, 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.
Pageof 18