Fonte: Journal of bone and mineral research. Nome do evento: Annual Meeting of the American-Society-for-Bone-and-Mineral-Research (ASBMR). Unidade: FM
Assuntos: OSTEOPOROSE, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
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ROCHA-BRAZ, Manuela et al. Targeted Massively Parallel Sequencing of 128 Candidate Genes Reveals a Potential Molecular Cause in 75% of Cases with Idiopathic, Severe or Familial Osteoporosis. Journal of bone and mineral research. Hoboken: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 07 ago. 2024. , 2017APA
Rocha-braz, M., França, M., Fernandes, A., Martin, R., Mendonça, B. B. de, & Souza, B. F. de. (2017). Targeted Massively Parallel Sequencing of 128 Candidate Genes Reveals a Potential Molecular Cause in 75% of Cases with Idiopathic, Severe or Familial Osteoporosis. Journal of bone and mineral research. Hoboken: Faculdade de Medicina, Universidade de São Paulo.NLM
Rocha-braz M, França M, Fernandes A, Martin R, Mendonça BB de, Souza BF de. Targeted Massively Parallel Sequencing of 128 Candidate Genes Reveals a Potential Molecular Cause in 75% of Cases with Idiopathic, Severe or Familial Osteoporosis. Journal of bone and mineral research. 2017 ; 32 S372-S372.[citado 2024 ago. 07 ]Vancouver
Rocha-braz M, França M, Fernandes A, Martin R, Mendonça BB de, Souza BF de. Targeted Massively Parallel Sequencing of 128 Candidate Genes Reveals a Potential Molecular Cause in 75% of Cases with Idiopathic, Severe or Familial Osteoporosis. Journal of bone and mineral research. 2017 ; 32 S372-S372.[citado 2024 ago. 07 ]
