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King-Smith

Showing results (161-170 of 176) with videos related to

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Human Mutation|August 13, 2021
GATA2 deficiency syndrome: A decade of discoveryClaire C Homan, Parvathy Venugopal, Peer Arts, et al.
BMC Medical Genomics|February 28, 2021
Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopiaCarla De Angelis, Alicia B Byrne, Rebecca Morrow, et al.
American Journal of Medical Genetics. Part A|March 7, 2020
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndromePeer Arts, Jessica Garland, Alicia B Byrne, et al.
Nature Communications|November 3, 2023
Glycoengineered keratinocyte library reveals essential functions of specific glycans for all stages of HSV-1 infectionIeva Bagdonaite, Irina N Marinova, Asha M Rudjord-Levann, et al.
Journal of Medical Genetics|January 29, 2020
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesisAlicia B Byrne, Shuji Mizumoto, Peer Arts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2020
Parental experiences of ultrarapid genomic testing for their critically unwell infants and childrenGemma R Brett, Melissa Martyn, Fiona Lynch, et al.
Blood Advances|May 10, 2022
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutationsMichael W Drazer, Claire C Homan, Kai Yu, et al.
Nature Medicine|January 19, 2023
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Nature Medicine|July 10, 2023
Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Haematologica|July 8, 2021
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancyClaire C Homan, Sarah L King-Smith, David M Lawrence, et al.
Pageof 18

Showing results (161-170 of 176) with videos related to

Sort By:
Pageof 18
Human Mutation|August 13, 2021
GATA2 deficiency syndrome: A decade of discoveryClaire C Homan, Parvathy Venugopal, Peer Arts, et al.
BMC Medical Genomics|February 28, 2021
Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopiaCarla De Angelis, Alicia B Byrne, Rebecca Morrow, et al.
American Journal of Medical Genetics. Part A|March 7, 2020
Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndromePeer Arts, Jessica Garland, Alicia B Byrne, et al.
Nature Communications|November 3, 2023
Glycoengineered keratinocyte library reveals essential functions of specific glycans for all stages of HSV-1 infectionIeva Bagdonaite, Irina N Marinova, Asha M Rudjord-Levann, et al.
Journal of Medical Genetics|January 29, 2020
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesisAlicia B Byrne, Shuji Mizumoto, Peer Arts, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2020
Parental experiences of ultrarapid genomic testing for their critically unwell infants and childrenGemma R Brett, Melissa Martyn, Fiona Lynch, et al.
Blood Advances|May 10, 2022
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutationsMichael W Drazer, Claire C Homan, Kai Yu, et al.
Nature Medicine|January 19, 2023
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Nature Medicine|July 10, 2023
Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal deathAlicia B Byrne, Peer Arts, Thuong T Ha, et al.
Haematologica|July 8, 2021
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancyClaire C Homan, Sarah L King-Smith, David M Lawrence, et al.
Pageof 18