• A boy with Silver-Russell syndrome and Sotos syndrome
• A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of Sotos syndrome
• An adult female with 5q34-q35.2 deletion: A rare syndromic presentation of left ventricular non-compaction and congenital heart disease
• Application of array comparative genomic hybridization in prenatal diagnosis of a case with 5q35 deletion syndrome
• Characterization of a Rare Mosaicism in Autosomal Translocation of t(5;21) Using Conventional Cytogenetics and FISH Methods
• Defining the phenotype associated with microduplication reciprocal to Sotos syndrome microdeletion
• Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia
• Developmental retardation due to paternal 5q/11q translocation in a Chinese infant: clinical, chromosomal and microarray characterization
• Genetic defects of chromosome 5q and 7q in myeloid neoplasms
• Hyperinsulinemic hypoglycemia of infancy in Sotos syndrome
• Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort
• Low-level mosaicism of a de novo derivative chromosome 9 from a t(5;9)(q35.1;q34.3) has a major phenotypic impact
• Microarray delineation of familial chromosomal imbalance with deletion 5q35 and duplication 10q25 in a child showing multiple anomalies and dysmorphism
• NSD1 duplication in Silver-Russell syndrome (SRS): molecular karyotyping in patients with SRS features
• Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome
• Switch in FGFR3 and -4 expression profile during human renal development may account for transient hypercalcemia in patients with Sotos syndrome due to 5q35 microdeletions