Ali, Taccyanna M.; Linnenkamp, Bianca D. W.; Yamamoto, Guilherme L.; Honjo, Rachel S.; Menezes Filho, Hamilton Cabral de; Kim, Chong Ae 
; Bertola, Debora R.
Source: American journal of medical genetics part a. Unidade: FM
Subjects: FRATURAS, ANCESTRAIS, PREVALÊNCIA, FENÓTIPOS
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ALI, Taccyanna M. et al. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry. American journal of medical genetics part a, v. 188, n. 5, p. 1545-1549, 2022Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.62651. Acesso em: 23 maio 2024.APA
Ali, T. M., Linnenkamp, B. D. W., Yamamoto, G. L., Honjo, R. S., Menezes Filho, H. C. de, Kim, C. A., & Bertola, D. R. (2022). The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry. American journal of medical genetics part a, 188( 5), 1545-1549. doi:10.1002/ajmg.a.62651NLM
Ali TM, Linnenkamp BDW, Yamamoto GL, Honjo RS, Menezes Filho HC de, Kim CA, Bertola DR. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry [Internet]. American journal of medical genetics part a. 2022 ; 188( 5): 1545-1549.[citado 2024 maio 23 ] Available from: https://doi.org/10.1002/ajmg.a.62651Vancouver
Ali TM, Linnenkamp BDW, Yamamoto GL, Honjo RS, Menezes Filho HC de, Kim CA, Bertola DR. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry [Internet]. American journal of medical genetics part a. 2022 ; 188( 5): 1545-1549.[citado 2024 maio 23 ] Available from: https://doi.org/10.1002/ajmg.a.62651
