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1Academic Journal
المؤلفون: Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Randolph, Linda M, Chase, John M, Matas Aguilera, Maria J, Siles, Juan López, Church, Joseph A, Hauser, Natalie, Shen, Joseph J, Jones, Marilyn C, Wierenga, Klaas J, Jiang, Zhijie, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan
المصدر: European Journal of Human Genetics. 23(5)
مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Brain Disorders, Intellectual and Developmental Disabilities (IDD), Clinical Research, Rare Diseases, Adolescent, Adult, Child, Child, Preschool, Chromosome Aberrations, Consanguinity, Family, Female, Genes, Recessive, Genetic Association Studies, Genetic Predisposition to Disease, Homozygote, Humans, Incidence, Inflammatory Bowel Diseases, Male, Oligonucleotide Array Sequence Analysis, Polymorphism, Single Nucleotide, Young Adult, Clinical Sciences, Genetics & Heredity, Clinical sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/5zs0k50h
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2Academic Journal
المؤلفون: Wang, Jia-Chi, Ross, Leslie, Mahon, Loretta W, Owen, Renius, Hemmat, Morteza, Wang, Boris T, El Naggar, Mohammed, Kopita, Kimberly A, Randolph, Linda M, Chase, John M, Matas Aguilera, Maria J, Siles, Juan López, Church, Joseph A, Hauser, Natalie, Shen, Joseph J, Jones, Marilyn C, Wierenga, Klaas J, Jiang, Zhijie, Haddadin, Mary, Boyar, Fatih Z, Anguiano, Arturo, Strom, Charles M, Sahoo, Trilochan
المصدر: European Journal of Human Genetics ; volume 23, issue 5, page 663-671 ; ISSN 1018-4813 1476-5438