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chd7 protein, human
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Neural crest cells derived from iPSCs of CHARGE syndrome patients with CHD7 mutations
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Clinical and genetic analysis of two patients with CHARGE syndrome due to de novo variants of CHD7 g…
Analysis of CHD7 gene variants in 22 patients with idiopathic hypogonadotropic hypogonadism].
Generation of a human iPSC line (FDCHi009-A) from a patient with CHARGE syndrome carrying a novel CH…
The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gen…
Novel noncanonical splice site variant causes mild CHD7-related disorder with variable intrafamilial…
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Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders
Phase I/II Thymus Transplantation With Immunosuppression #950
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