Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Katia Sol-Church

Showing results (31-40 of 68) with videos related to

Pageof 7
Sort By:
American Journal of Medical Genetics. Part A|June 15, 2007
Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndromeMohamad M Al-Rahawan, Deborah J Chute, Katia Sol-Church, et al.
American Journal of Medical Genetics. Part A|June 20, 2014
Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28Karen W Gripp, Cynthia Curry, Ann Haskins Olney, et al.
Frontiers in Oncology|April 20, 2017
Cytotoxicity of Zardaverine in Embryonal Rhabdomyosarcoma from a Costello Syndrome PatientDonna M Cartledge, Katherine M Robbins, Katherine M Drake, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 19, 2014
Early-lethal Costello syndrome due to rare HRAS Tandem Base substitution (c.35_36GC>AA; p.G12E)-associated pulmonary vascular diseaseK Nicole Weaver, Dehua Wang, James Cnota, et al.
The Journal of Infection|June 18, 2026
Multi-strain Clostridioides difficile infection: Increased Detection and Clinical ImplicationsMônica J Rodrigues-Jesus, Maria L G S Morais, Jae Hyun Shin, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosisKaren W Gripp, Dina J Zand, Laurie Demmer, et al.
Pediatric Blood & Cancer|March 3, 2015
A phase I trial and viral clearance study of reovirus (Reolysin) in children with relapsed or refractory extra-cranial solid tumors: a Children's Oncology Group Phase I Consortium reportE Anders Kolb, Valerie Sampson, Deborah Stabley, et al.
Journal of Biomolecular Techniques : JBT|March 13, 2023
Rigor, Reproducibility, and Transparency in Shared Research Resources: Follow-Up Survey and Recommendations for ImprovementsAndrew W Ott, Katia Sol-Church, Gauravi M Deshpande, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hairKaren W Gripp, Kimberly A Aldinger, James T Bennett, et al.
JCI Insight|March 15, 2017
Elucidation of <i>MRAS</i>-mediated Noonan syndrome with cardiac hypertrophyErin M Higgins, J Martijn Bos, Heather Mason-Suares, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part A|June 15, 2007
Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndromeMohamad M Al-Rahawan, Deborah J Chute, Katia Sol-Church, et al.
American Journal of Medical Genetics. Part A|June 20, 2014
Diamond-Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28Karen W Gripp, Cynthia Curry, Ann Haskins Olney, et al.
Frontiers in Oncology|April 20, 2017
Cytotoxicity of Zardaverine in Embryonal Rhabdomyosarcoma from a Costello Syndrome PatientDonna M Cartledge, Katherine M Robbins, Katherine M Drake, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 19, 2014
Early-lethal Costello syndrome due to rare HRAS Tandem Base substitution (c.35_36GC>AA; p.G12E)-associated pulmonary vascular diseaseK Nicole Weaver, Dehua Wang, James Cnota, et al.
The Journal of Infection|June 18, 2026
Multi-strain Clostridioides difficile infection: Increased Detection and Clinical ImplicationsMônica J Rodrigues-Jesus, Maria L G S Morais, Jae Hyun Shin, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosisKaren W Gripp, Dina J Zand, Laurie Demmer, et al.
Pediatric Blood & Cancer|March 3, 2015
A phase I trial and viral clearance study of reovirus (Reolysin) in children with relapsed or refractory extra-cranial solid tumors: a Children's Oncology Group Phase I Consortium reportE Anders Kolb, Valerie Sampson, Deborah Stabley, et al.
Journal of Biomolecular Techniques : JBT|March 13, 2023
Rigor, Reproducibility, and Transparency in Shared Research Resources: Follow-Up Survey and Recommendations for ImprovementsAndrew W Ott, Katia Sol-Church, Gauravi M Deshpande, et al.
American Journal of Medical Genetics. Part A|June 7, 2016
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hairKaren W Gripp, Kimberly A Aldinger, James T Bennett, et al.
JCI Insight|March 15, 2017
Elucidation of <i>MRAS</i>-mediated Noonan syndrome with cardiac hypertrophyErin M Higgins, J Martijn Bos, Heather Mason-Suares, et al.
Pageof 7