Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?
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A. Poustka | M. Pembrey | L. Villard | M. Fontès | M. Till | S. Odent | A. Guichet | J. Lucas | J. Coy | A. Shrimpton | S. Briault | C. Moraine | E. Passage | U. Rogner | D. Zhu | S. Dessay