Recurrent reciprocal 1q21.1 deletions and duplications are novel genomic disorders associated with micro- or macrocephaly and a spectrum of developmental and behavioral abnormalities / BRUNETTI PIERRI, Nicola; Berg, Js; Scaglia, F; Belmont, J; Bacino, Ca; Sahoo, T; Lalani, Sr; Graham, H; Lee, B; Shinawi, M; Shen, J; Kang S., Hl; Pursley, A; Lotze, T; Kennedy, G; Lansky Shafer, S; Weaver, C; Roeder, Er; Grebe, Ta; Arnold, Gl; Hutchison, T; Reimschisel, T; Amato, S; Geragthy, Mt; Innis, Jw; Obersztyn, E; Nowakowska, B; Rosengren, Ss; Bader, Pi; Grange, Dk; Naqvi, S; Garnica, Ad; Bernes, Sm; Fong, C. T.; Summers, A; Walters, Wd; Lupski, Jr; Stankiewicz, P; Cheung, S. W.; Patel, A.. - In: NATURE GENETICS. - ISSN 1061-4036. - STAMPA. - 40:12(2008), pp. 1466-1471.

Recurrent reciprocal 1q21.1 deletions and duplications are novel genomic disorders associated with micro- or macrocephaly and a spectrum of developmental and behavioral abnormalities.

BRUNETTI PIERRI, NICOLA;
2008

2008
Recurrent reciprocal 1q21.1 deletions and duplications are novel genomic disorders associated with micro- or macrocephaly and a spectrum of developmental and behavioral abnormalities / BRUNETTI PIERRI, Nicola; Berg, Js; Scaglia, F; Belmont, J; Bacino, Ca; Sahoo, T; Lalani, Sr; Graham, H; Lee, B; Shinawi, M; Shen, J; Kang S., Hl; Pursley, A; Lotze, T; Kennedy, G; Lansky Shafer, S; Weaver, C; Roeder, Er; Grebe, Ta; Arnold, Gl; Hutchison, T; Reimschisel, T; Amato, S; Geragthy, Mt; Innis, Jw; Obersztyn, E; Nowakowska, B; Rosengren, Ss; Bader, Pi; Grange, Dk; Naqvi, S; Garnica, Ad; Bernes, Sm; Fong, C. T.; Summers, A; Walters, Wd; Lupski, Jr; Stankiewicz, P; Cheung, S. W.; Patel, A.. - In: NATURE GENETICS. - ISSN 1061-4036. - STAMPA. - 40:12(2008), pp. 1466-1471.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/363126
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