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Trinucleotide repeats are prevalent among cancer-related genes.
Trends in genetics : TIG Jan, 2008 | Pubmed ID: 18054813
Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations.
European journal of human genetics : EJHG 08, 2016 | Pubmed ID: 26883093
Expanding the molecular diversity and phenotypic spectrum of glycerol 3-phosphate dehydrogenase 1 deficiency.
Journal of inherited metabolic disease Sep, 2016 | Pubmed ID: 27368975
Congenital Sucrase-isomaltase Deficiency: A Novel Compound Heterozygous Mutation Causing Aberrant Protein Localization.
Journal of pediatric gastroenterology and nutrition May, 2017 | Pubmed ID: 27749612
Mucosal Expression of Type 2 and Type 17 Immune Response Genes Distinguishes Ulcerative Colitis From Colon-Only Crohn's Disease in Treatment-Naive Pediatric Patients.
Gastroenterology May, 2017 | Pubmed ID: 28132889
Fecal microbial characterization of hospitalized patients with suspected infectious diarrhea shows significant dysbiosis.
Scientific reports Apr, 2017 | Pubmed ID: 28439072
Impaired IL-10 Receptor Mediated Suppression in Monocyte from Patients with Crohn's Disease.
Journal of pediatric gastroenterology and nutrition Oct, 2017 | Pubmed ID: 29045353
Long ncRNA Landscape in the Ileum of Treatment-Naive Early-Onset Crohn Disease.
Inflammatory bowel diseases Jan, 2018 | Pubmed ID: 29361088
Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric Syndrome.
Digestive diseases and sciences Feb, 2018 | Pubmed ID: 29484573
Sheba Medical Center
Cincinnati Children's Hospital Medical Center
Ayelet Di Segni1,
Tzipi Braun1,
Marina BenShoshan1,
Sarit Farage Barhom1,
Efrat Glick Saar1,
Karen Cesarkas1,
James E. Squires2,
Nathan Keller1,3,
Yael Haberman1,4
1, Sheba Medical Center,
2, Children's Hospital of Pittsburgh of UPMC,
3, Ariel University,
4, Cincinnati Children's Hospital Medical Center
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