Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study
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D. Loesch | J. Hopper | C. Skinner | C. Schwartz | Q. Bui | S. Metcalfe | R. Hagerman | D. Francis | D. Amor | H. Slater | J. Hewitt | J. Cohen | A. Herlihy | Tiffany L Wotton | D. Godler | K. Pope | Yoshimi Inaba | E. Shi | Joanna Cobb | A. Arvaj