CÉLULAS MADRE Y TERAPIA CELULAR
University of Erlangen-Nuremberg
Erlangen, AlemaniaPublications en collaboration avec des chercheurs de University of Erlangen-Nuremberg (2)
2013
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A comprehensive molecular study on coffin-siris and nicolaides-baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
Human Molecular Genetics, Vol. 22, Núm. 25, pp. 5121-5135
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MLL2 mutation detection in 86 patients with Kabuki syndrome: A genotype-phenotype study
Clinical Genetics, Vol. 84, Núm. 6, pp. 539-545