A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion - Concepedia

Concepedia

Publication | Closed Access

A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion

62

Citations

14

References

2014

Year

European Journal of Medical Genetics

Mendelian DisorderKorean FamilyAnkrd11 MutationGenetic DisorderGeneticsPathologyMolecular GeneticsDisease Gene IdentificationKbg SyndromeMedicine

References

	Year	Citations

Page 1