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Browsing by Author Abdulsamad Wafa

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