Ullmann, Reinhard; Turner, Gillian; Kirchhoff, Maria; Chen, Wei; Tonge, Bruce; Rosenberg, Carla 
; Field, Michael; Vianna-Morgante, Angela M ; Christie, Louise; Krepischi, Ana Cristina Victorino ; Banna, Lynn; Brereton, Avril V.; Hill, Alyssa; Bisgaard, Anne-Marie; Müller, Ines; Hultschig, Claus; Erdogan, Fikret; Wieczorek, Georg; Ropers, H. Hilger
Source: Human Mutation. Unidade: IB
Subjects: RETARDO MENTAL, CROMOSSOMOS HUMANOS (ANOMALIAS)
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ULLMANN, Reinhard et al. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutation, v. 28, n. 7, p. 674-682, 2007Tradução . . Disponível em: https://doi.org/10.1002/humu.20546. Acesso em: 13 nov. 2024.APA
Ullmann, R., Turner, G., Kirchhoff, M., Chen, W., Tonge, B., Rosenberg, C., et al. (2007). Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutation, 28( 7), 674-682. doi:10.1002/humu.20546NLM
Ullmann R, Turner G, Kirchhoff M, Chen W, Tonge B, Rosenberg C, Field M, Vianna-Morgante AM, Christie L, Krepischi ACV, Banna L, Brereton AV, Hill A, Bisgaard A-M, Müller I, Hultschig C, Erdogan F, Wieczorek G, Ropers HH. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation [Internet]. Human Mutation. 2007 ; 28( 7): 674-682.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/humu.20546Vancouver
Ullmann R, Turner G, Kirchhoff M, Chen W, Tonge B, Rosenberg C, Field M, Vianna-Morgante AM, Christie L, Krepischi ACV, Banna L, Brereton AV, Hill A, Bisgaard A-M, Müller I, Hultschig C, Erdogan F, Wieczorek G, Ropers HH. Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation [Internet]. Human Mutation. 2007 ; 28( 7): 674-682.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/humu.20546
