Variome And NotGabriela Möslein

List of bibliographic references

Number of relevant bibliographic references: 2.

Ident.	Authors (with country if any)	Title
001728	Marc S. Greenblatt [États-Unis] ; Lawrence C. Brody [États-Unis] ; William D. Foulkes [Canada] ; Maurizio Genuardi [Italie] ; Robert M. W. Hofstra [Pays-Bas] ; Magali Olivier [France] ; Sharon E. Plon [États-Unis] ; Rolf H. Sijmons [Pays-Bas] ; Olga Sinilnikova [France] ; Amanda B. Spurdle [Australie]	Locus‐specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes
001852	R. G. H. Cotton [Australie] ; A. D. Auerbach [États-Unis] ; A. F. Brown [Royaume-Uni] ; P. Carrera [Italie] ; J. Christodoulou [Australie] ; M. Claustres [France] ; J. Compton [États-Unis] ; D. W. Cox [Canada] ; E. De Baere [Belgique] ; J. T. Den Dunnen ; M. Greenblatt [États-Unis] ; M. Fujiwara [Canada] ; P. Hilbert [Belgique] ; A. Jani [Royaume-Uni] ; H. Lehvaslaiho [Afrique du Sud] ; D. W. Nebert [États-Unis] ; I. Verma [Inde] ; M. Vihinen [Finlande]	A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases

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