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Rare variants in single-minded 1 (SIM1) areassociated with severe obesity.
Rare variants in single-minded 1 (SIM1) are associated with severe obesity
Large, rare chromosomal deletions associated with severe early-onset obesity
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance
Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis
Clinical dividends from the molecular genetic diagnosis of craniosynostosis
Genomic studies of gene expression: regulation of the Wilson disease gene
