Towards mapping phenotypical traits in 18p− syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation
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A. Hoischen | D. Wieczorek | P. Propping | H. Engels | B. Radlwimmer | G. Gillessen‐kaesbach | E. Prott | R. Weber | C. Walldorf | D. Trost | C. Brenk | G. Gillessen‐Kaesbach | Constanze Walldorf
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