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Aniko Sabo

Showing results (11-20 of 52) with videos related to

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Human Molecular Genetics|June 1, 2011
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disordersChristian P Schaaf, Aniko Sabo, Yasunari Sakai, et al.
American Journal of Medical Genetics. Part A|February 25, 2026
Double Mosaicism in Xia-Gibbs SyndromeJianhong Hu, Moez Dawood, Heer Hemant Mehta, et al.
Obesity (Silver Spring, Md.)|May 17, 2017
Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic childrenAniko Sabo, Pamela Mishra, Shannon Dugan-Perez, et al.
Blood Advances|June 8, 2023
Identification of USP9X as a leukemia susceptibility geneSaumya Dushyant Sisoudiya, Pamela Mishra, He Li, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delayAyşegül Ozantürk, Erica E Davis, Aniko Sabo, et al.
American Journal of Human Genetics|June 15, 2021
Exome variant discrepancies due to reference-genome differencesHe Li, Moez Dawood, Michael M Khayat, et al.
Life Science Alliance|July 24, 2021
Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplantMarie-Claude Gingras, Aniko Sabo, Maria Cardenas, et al.
Pediatric Blood & Cancer|May 17, 2023
TP53 germline pathogenic variant frequency in anaplastic rhabdomyosarcoma: A Children's Oncology Group reportDouglas Fair, Luke Maese, Yueh-Yun Chi, et al.
Plos One|November 1, 2014
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemiaVivien A Sheehan, Jacy R Crosby, Aniko Sabo, et al.
Pediatric Diabetes|August 13, 2021
Exome sequencing in children with clinically suspected maturity-onset diabetes of the youngMustafa Tosur, Claudia Soler-Alfonso, Katie M Chan, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|June 1, 2011
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disordersChristian P Schaaf, Aniko Sabo, Yasunari Sakai, et al.
American Journal of Medical Genetics. Part A|February 25, 2026
Double Mosaicism in Xia-Gibbs SyndromeJianhong Hu, Moez Dawood, Heer Hemant Mehta, et al.
Obesity (Silver Spring, Md.)|May 17, 2017
Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic childrenAniko Sabo, Pamela Mishra, Shannon Dugan-Perez, et al.
Blood Advances|June 8, 2023
Identification of USP9X as a leukemia susceptibility geneSaumya Dushyant Sisoudiya, Pamela Mishra, He Li, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delayAyşegül Ozantürk, Erica E Davis, Aniko Sabo, et al.
American Journal of Human Genetics|June 15, 2021
Exome variant discrepancies due to reference-genome differencesHe Li, Moez Dawood, Michael M Khayat, et al.
Life Science Alliance|July 24, 2021
Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplantMarie-Claude Gingras, Aniko Sabo, Maria Cardenas, et al.
Pediatric Blood & Cancer|May 17, 2023
TP53 germline pathogenic variant frequency in anaplastic rhabdomyosarcoma: A Children's Oncology Group reportDouglas Fair, Luke Maese, Yueh-Yun Chi, et al.
Plos One|November 1, 2014
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemiaVivien A Sheehan, Jacy R Crosby, Aniko Sabo, et al.
Pediatric Diabetes|August 13, 2021
Exome sequencing in children with clinically suspected maturity-onset diabetes of the youngMustafa Tosur, Claudia Soler-Alfonso, Katie M Chan, et al.
Pageof 6