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1.
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defects.
Clin Genet;
100(3): 268-279, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-33988253
2.
Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group.
JCO Precis Oncol;
22018.
Artículo
en Inglés
| MEDLINE | ID: mdl-31517176
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