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Browsing by Author Suher Almedani, Thomas Liehr

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Issue Date	Title	Author(s)
2020	A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome	Abdulsamad Wafa, Faten Moassass; Suher Almedani, Thomas Liehr; Kathleen Wilhelm

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