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Article

17q21.31 microdeletion in a patient with pituitary stalk interruption syndrome

11 Mar 2011

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 21397059
DOI: 10.1016/j.ejmg.2011.03.001

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Re-analysis of gene mutations found in pituitary stalk interruption syndrome and a new hypothesis on the etiology.Semantic proximity Read ↗

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Clinical and molecular delineation of the 17q21.31 microdeletion syndrome.Semantic proximity Read ↗

Pituitary stalk interruption syndrome in 58 Chinese patients: clinical features and genetic analysis.Semantic proximity Read ↗

Molecular Characterization and Gene Content of Breakpoint Boundaries in Patients with Neurofibromatosis Type 1 with 17q11.2 MicrodeletionsSemantic proximity Read ↗

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