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Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.Academic Article Why?
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.Academic Article Why?
Neurodevelopmental DisordersConcept Why?
Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin.Academic Article Why?
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 Why?
Childhood Outcomes Following Parechovirus Infections in a US Young Infant Cohort.Academic Article Why?
De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype.Academic Article Why?
High-resolution analyses of human sperm dynamic methylome reveal thousands of novel age-related epigenetic alterations.Academic Article Why?
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 Why?
Lane, RobertPerson Why?
Nadler, CyPerson Why?
Recurrent FOXP4 nonsense variant in two unrelated patients: Association with neurodevelopmental disease and congenital diaphragmatic hernia.Academic Article Why?
Selvarangan, RangarajPerson Why?
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.Academic Article Why?
Higher or Lower Hemoglobin Transfusion Thresholds for Preterm Infants.Academic Article Why?
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