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Carolyn R Raski

Showing results (1-10 of 6) with videos related to

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American Journal of Medical Genetics. Part A|November 11, 2025
Syndrome of the Month: An Update on Smith-Kingsmore Syndrome: Characterization of Developmental Milestones and a Review of the LiteratureCarolyn R Raski, Carlos E Prada
American Journal of Medical Genetics. Part A|May 18, 2024
Dandy-Walker malformation in an individual with ABL1 variantJenny P Garzon, Andrea C Pardo, Carolyn R Raski, et al.
American Journal of Medical Genetics. Part A|May 9, 2024
Aminotransferase trends in propionic acidemiaMaria P Silva, Carolyn R Raski, Joel Charrow, et al.
American Journal of Medical Genetics. Part A|August 29, 2025
Sacroiliac Joint Involvement: An Underreported Complication of NF1Jenny P Garzon, Eva Dombi, Jonathan Samet, et al.
American Journal of Medical Genetics. Part A|September 11, 2024
Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New IndividualsAnne M McRae, Jaime Duncan, Andy Drackley, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 18, 2024
Expanding the phenotype of neurofibromatosis type 1 microdeletion syndromeJenny P Garzon, Andrea Patete, Lindsey Aschbacher-Smith, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|November 11, 2025
Syndrome of the Month: An Update on Smith-Kingsmore Syndrome: Characterization of Developmental Milestones and a Review of the LiteratureCarolyn R Raski, Carlos E Prada
American Journal of Medical Genetics. Part A|May 18, 2024
Dandy-Walker malformation in an individual with ABL1 variantJenny P Garzon, Andrea C Pardo, Carolyn R Raski, et al.
American Journal of Medical Genetics. Part A|May 9, 2024
Aminotransferase trends in propionic acidemiaMaria P Silva, Carolyn R Raski, Joel Charrow, et al.
American Journal of Medical Genetics. Part A|August 29, 2025
Sacroiliac Joint Involvement: An Underreported Complication of NF1Jenny P Garzon, Eva Dombi, Jonathan Samet, et al.
American Journal of Medical Genetics. Part A|September 11, 2024
Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New IndividualsAnne M McRae, Jaime Duncan, Andy Drackley, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 18, 2024
Expanding the phenotype of neurofibromatosis type 1 microdeletion syndromeJenny P Garzon, Andrea Patete, Lindsey Aschbacher-Smith, et al.
Pageof 1