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Publications by Peter Wieacker

Severe XIST Hypomethylation Clearly Distinguishes (SRY+) 46,xx-Maleness From Klinefelter Syndrome

European Journal of Endocrinology

English

Dissecting the Molecular Mechanisms in Craniofrontonasal Syndrome: Differential mRNA Expression of Mutant EFNB1 and the Cellular Mosaic

European Journal of Human Genetics

English