Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome - Concepedia

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Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

DOI Full Paper Access

330

Citations

38

References

2008

Year

Hyung‐Goo Kim, Ingo Kurth, Fei Lan, Irene Meliciani, Wolfgang Wenzel, Soo Hyun Eom, Gil Bu Kang, Georg Rosenberger, Mustafa Tekin, Metin Özata,

The American Journal of Human Genetics

Chromatin-remodeling ProteinChromatinDevelopmental BiologyChromatin StructureChromatin RemodelingGenetic DisorderEpigenetic ChangeGeneticsMendelian DisorderKallmann SyndromeChromosome BiologyMolecular GeneticsEndocrinologyMedicineEpigeneticsDisorders Of Sex Development

References

	Year	Citations

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