Abstract #989420: A Novel CHD7 Mutation, Described as a Variant of Uncertain Significance, is Found in a Patient Diagnosed with Kallmann Syndrome

Abouzid, Mohamed; Riad, Mohamed; Zaidi, Syeda S.; Dueñas, José; Rendón, Maria; Yadav, Ritu; Singh, Jasveer; Mirza, Lubna

doi:10.1016/j.eprac.2021.04.699

Endocrine Practice

2021

DOI: 10.1016/j.eprac.2021.04.699

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Abstract #989420: A Novel CHD7 Mutation, Described as a Variant of Uncertain Significance, is Found in a Patient Diagnosed with Kallmann Syndrome

Mohamed Abouzid

Mohamed Riad

Syeda S. Zaidi

et al.

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Abstract #989420: A Novel CHD7 Mutation, Described as a Variant of Uncertain Significance, is Found in a Patient Diagnosed with Kallmann Syndrome

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See others like this or search for similar articles

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