Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome
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A. Bassett | Z. Demko | J. Babiarz | D. McDonald-McGinn | E. Kırkızlar | B. Zimmermann | M. Stosic | S. Gross | N. Wayham | A. Ryan | Kristine N. Jinnett | P. Benn | A. Bassett | K. Kobara | K. N. Jinnett | A. Norvez | R. Dhamankar | Joshua Babiarz | Katie Kobara | Nicholas Wayham