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American Journal of Medical Genetics. Part A
|
February 14, 2018
Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome
Yuri A Zarate, Constance L Smith-Hicks, Carol Greene, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 15, 2019
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder
Ghayda M Mirzaa, Jessica X Chong, Amélie Piton, et al.
American Journal of Human Genetics
|
April 17, 2018
Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies
Hanyin Cheng, Avinash V Dharmadhikari, Sylvia Varland, et al.
Nature Communications
|
February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
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of 4
Search research articles
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Showing results (31-40 of 34) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 34 results.
American Journal of Medical Genetics. Part A
|
February 14, 2018
Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome
Yuri A Zarate, Constance L Smith-Hicks, Carol Greene, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 15, 2019
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder
Ghayda M Mirzaa, Jessica X Chong, Amélie Piton, et al.
American Journal of Human Genetics
|
April 17, 2018
Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies
Hanyin Cheng, Avinash V Dharmadhikari, Sylvia Varland, et al.
Nature Communications
|
February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
Holger Hengel, Célia Bosso-Lefèvre, George Grady, et al.
Page
of 4