Publication | Closed Access
Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome
281
Citations
26
References
2006
Year
Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsClinical GeneticsSheldon-hall SyndromeFreeman-sheldon SyndromeMolecular GeneticsDisease Gene IdentificationMedicineMonogenic Disorders
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