Search Results (29)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders. | Academic Article |
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| Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders. | Academic Article |
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| Neurodevelopmental Disorders | Concept |
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| Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin. | Academic Article |
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| A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the TRPM1, CHRNA7, and other homozygously deleted genes. | Academic Article |
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| Childhood Outcomes Following Parechovirus Infections in a US Young Infant Cohort. | Academic Article |
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| De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype. | Academic Article |
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| High-resolution analyses of human sperm dynamic methylome reveal thousands of novel age-related epigenetic alterations. | Academic Article |
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| Initial Laparotomy Versus Peritoneal Drainage in Extremely Low Birthweight Infants With Surgical Necrotizing Enterocolitis or Isolated Intestinal Perforation: A Multicenter Randomized Clinical Trial. | Academic Article |
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| Lane, Robert | Person |
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| Nadler, Cy | Person |
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| Recurrent FOXP4 nonsense variant in two unrelated patients: Association with neurodevelopmental disease and congenital diaphragmatic hernia. | Academic Article |
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| Selvarangan, Rangaraj | Person |
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| CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. | Academic Article |
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| Higher or Lower Hemoglobin Transfusion Thresholds for Preterm Infants. | Academic Article |
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