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

Stephen F Kingsmore

Showing results (31-40 of 171) with videos related to

Pageof 18
Sort By:
Orphanet Journal of Rare Diseases|October 19, 2013
Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinismLaura Dotta, Silvia Parolini, Alberto Prandini, et al.
Annals of Medicine|November 2, 2011
Perinatal immunoproteins predict the risk of cerebral palsy in preterm childrenTuula Kaukola, Hanna Kallankari, Jarno Tuimala, et al.
Cytokine|February 4, 2011
Cord blood chemokines differentiate between spontaneous and elective preterm births in singleton pregnanciesTuula Kaukola, Marja Ojaniemi, Jarno Tuimala, et al.
Prenatal Diagnosis|February 10, 2022
Retrospective identification of prenatal fetal anomalies associated with diagnostic neonatal genomic sequencing resultsKathy Zhang-Rutledge, Mallory Owen, Nathaly M Sweeney, et al.
Cold Spring Harbor Molecular Case Studies|November 9, 2018
Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhageBenjamin Briggs, Kiely N James, Shimul Chowdhury, et al.
Annals of Medicine|July 9, 2010
Chemokine CCL18 predicts intraventricular hemorrhage in very preterm infantsHanna Kallankari, Tuula Kaukola, Marja Ojaniemi, et al.
Cold Spring Harbor Molecular Case Studies|September 3, 2017
Rapid whole-genome sequencing identifies a novel <i>GABRA1</i> variant associated with West syndromeLauge Farnaes, Shareef A Nahas, Shimul Chowdhury, et al.
Plos One|January 26, 2023
The Genomic landscape of short tandem repeats across multiple ancestriesPrashanth Vijayaraghavan, Sergey Batalov, Yan Ding, et al.
Frontiers in Pediatrics|March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary systemErika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Cold Spring Harbor Molecular Case Studies|February 14, 2018
Rapid whole-genome sequencing identifies a novel <i>AIRE</i> variant associated with autoimmune polyendocrine syndrome type 1Erica Sanford, Kelly Watkins, Shareef Nahas, et al.
Pageof 18

Showing results (31-40 of 171) with videos related to

Sort By:
Pageof 18
Orphanet Journal of Rare Diseases|October 19, 2013
Clinical, laboratory and molecular signs of immunodeficiency in patients with partial oculo-cutaneous albinismLaura Dotta, Silvia Parolini, Alberto Prandini, et al.
Annals of Medicine|November 2, 2011
Perinatal immunoproteins predict the risk of cerebral palsy in preterm childrenTuula Kaukola, Hanna Kallankari, Jarno Tuimala, et al.
Cytokine|February 4, 2011
Cord blood chemokines differentiate between spontaneous and elective preterm births in singleton pregnanciesTuula Kaukola, Marja Ojaniemi, Jarno Tuimala, et al.
Prenatal Diagnosis|February 10, 2022
Retrospective identification of prenatal fetal anomalies associated with diagnostic neonatal genomic sequencing resultsKathy Zhang-Rutledge, Mallory Owen, Nathaly M Sweeney, et al.
Cold Spring Harbor Molecular Case Studies|November 9, 2018
Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhageBenjamin Briggs, Kiely N James, Shimul Chowdhury, et al.
Annals of Medicine|July 9, 2010
Chemokine CCL18 predicts intraventricular hemorrhage in very preterm infantsHanna Kallankari, Tuula Kaukola, Marja Ojaniemi, et al.
Cold Spring Harbor Molecular Case Studies|September 3, 2017
Rapid whole-genome sequencing identifies a novel <i>GABRA1</i> variant associated with West syndromeLauge Farnaes, Shareef A Nahas, Shimul Chowdhury, et al.
Plos One|January 26, 2023
The Genomic landscape of short tandem repeats across multiple ancestriesPrashanth Vijayaraghavan, Sergey Batalov, Yan Ding, et al.
Frontiers in Pediatrics|March 31, 2023
Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary systemErika T Allred, Elliot A Perens, Nicole G Coufal, et al.
Cold Spring Harbor Molecular Case Studies|February 14, 2018
Rapid whole-genome sequencing identifies a novel <i>AIRE</i> variant associated with autoimmune polyendocrine syndrome type 1Erica Sanford, Kelly Watkins, Shareef Nahas, et al.
Pageof 18