Source: Human Genetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEUROLOGIA
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JALALI, Ali et al. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics, v. 123, n. 3, p. 237-245, 2008Tradução . . Disponível em: https://doi.org/10.1007/s00439-008-0467-y. Acesso em: 16 nov. 2024.APA
Jalali, A., Aldinger, K. A., Chary, A., McLone, D. G., Bowman, R. M., Le, L. C., et al. (2008). Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics, 123( 3), 237-245. doi:10.1007/s00439-008-0467-yNLM
Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina Neto JM, Kessler JA, Bassuk AG. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity [Internet]. Human Genetics. 2008 ; 123( 3): 237-245.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00439-008-0467-yVancouver
Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina Neto JM, Kessler JA, Bassuk AG. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity [Internet]. Human Genetics. 2008 ; 123( 3): 237-245.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00439-008-0467-y
