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Human Molecular Genetics
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June 1, 2011
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders
Christian P Schaaf, Aniko Sabo, Yasunari Sakai, et al.
American Journal of Medical Genetics. Part A
|
February 25, 2026
Double Mosaicism in Xia-Gibbs Syndrome
Jianhong 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 children
Aniko Sabo, Pamela Mishra, Shannon Dugan-Perez, et al.
Blood Advances
|
June 8, 2023
Identification of USP9X as a leukemia susceptibility gene
Saumya 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 delay
Ayşegül Ozantürk, Erica E Davis, Aniko Sabo, et al.
American Journal of Human Genetics
|
June 15, 2021
Exome variant discrepancies due to reference-genome differences
He 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 transplant
Marie-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 report
Douglas 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 anemia
Vivien 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 young
Mustafa Tosur, Claudia Soler-Alfonso, Katie M Chan, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 6
Human Molecular Genetics
|
June 1, 2011
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders
Christian P Schaaf, Aniko Sabo, Yasunari Sakai, et al.
American Journal of Medical Genetics. Part A
|
February 25, 2026
Double Mosaicism in Xia-Gibbs Syndrome
Jianhong 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 children
Aniko Sabo, Pamela Mishra, Shannon Dugan-Perez, et al.
Blood Advances
|
June 8, 2023
Identification of USP9X as a leukemia susceptibility gene
Saumya 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 delay
Ayşegül Ozantürk, Erica E Davis, Aniko Sabo, et al.
American Journal of Human Genetics
|
June 15, 2021
Exome variant discrepancies due to reference-genome differences
He 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 transplant
Marie-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 report
Douglas 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 anemia
Vivien 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 young
Mustafa Tosur, Claudia Soler-Alfonso, Katie M Chan, et al.
Page
of 6