Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity - Concepedia

Concepedia

Publication | Open Access

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

DOI Full Paper Access

239

Citations

32

References

2010

Year

Ruxandra Bachmann‐Gagescu, Heather C. Mefford, Charles A. Cowan, Gwen M. Glew, Anne Hing, Stephanie E Wallace, Patricia I. Bader, Aline I. Hamati, Pamela J. Reitnauer, Rosemarie Smith,

Genetics in Medicine

Recurrent 200-Kb DeletionsDevelopmental BiologySh2b1 GeneGenetic DisorderGeneticsGenomic MechanismGene RegulationGene CharacterizationMolecular GeneticsGene ExpressionMedicineCell DevelopmentGene FunctionDevelopmental Delay

References

	Year	Citations

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