Shaw-Smith, Charles; Pittman, Alan M.; Willatt, Lionel; Martin, Howard; Rickman, Lisa; Gribble, Susan; Curley, Rebecca; Cumming, Sally; Dunn, Carolyn; Kalaitzopoulos, Dimitrios; Porter, Keith R.; Prigmore, Elena; Krepischi, Ana Cristina Victorino 
; Varela, Monica Castro; Koiffmann, Celia Priszkulnik ; Lees, Andrew J.; Rosenberg, Carla ; Firth, Helen V.; Silva, Rohan de; Carter, Nigel P.
Source: Nature Genetics. Unidade: IB
Subjects: ANORMALIDADES CROMOSSÔMICAS, MALFORMAÇÕES, GENÉTICA MÉDICA, DELEÇÃO DE GENES
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SHAW-SMITH, Charles et al. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nature Genetics, v. 38, n. 9, p. 1032-1037, 2006Tradução . . Disponível em: https://doi.org/10.1038/ng1858. Acesso em: 04 nov. 2024.APA
Shaw-Smith, C., Pittman, A. M., Willatt, L., Martin, H., Rickman, L., Gribble, S., et al. (2006). Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nature Genetics, 38( 9), 1032-1037. doi:10.1038/ng1858NLM
Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter KR, Prigmore E, Krepischi ACV, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, Silva R de, Carter NP. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability [Internet]. Nature Genetics. 2006 ; 38( 9): 1032-1037.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/ng1858Vancouver
Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter KR, Prigmore E, Krepischi ACV, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, Silva R de, Carter NP. Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability [Internet]. Nature Genetics. 2006 ; 38( 9): 1032-1037.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/ng1858
