Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
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M. Shoukier | J. Schröder | J. Gärtner | K. Brockmann | B. Zoll | P. Burfeind | P. Grzmil | B. Auber | B. Zirn | M. Lingen | E. Hobbiebrunken | E. A. Alsat | J. Wickert | I. Bartels | D. Weise | EA Alsat | N. Klein | S. Schulze | J. Keyser | M. Borchers | M. Röbl | EA Alsat