Johansen Taber, K., Lim‐Harashima, J., Naemi, H., & Goldberg, J. (2019). Fragile X syndrome carrier screening accompanied by genetic consultation has clinical utility in populations beyond those recommended by guidelines. Mol Genet Genomic Med.
Chicago-стиль цитированияJohansen Taber, Katherine, Jeraldine Lim‐Harashima, Harris Naemi, and Jim Goldberg. "Fragile X Syndrome Carrier Screening Accompanied By Genetic Consultation Has Clinical Utility in Populations Beyond Those Recommended By Guidelines." Mol Genet Genomic Med 2019.
MLA-цитированиеJohansen Taber, Katherine, Jeraldine Lim‐Harashima, Harris Naemi, and Jim Goldberg. "Fragile X Syndrome Carrier Screening Accompanied By Genetic Consultation Has Clinical Utility in Populations Beyond Those Recommended By Guidelines." Mol Genet Genomic Med 2019.