Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome
Hijazi, Hadia, Coelho, Fernanda S., Gonzaga‐Jauregui, Claudia, Bernardini, Laura, Mar, Soe S., Manning, Melanie A., Hanson‐Kahn, Andrea, Naidu, SakkuBai, Srivastava, Siddharth, Lee, Jennifer A., Jones, Julie R., Friez, Michael J., Alberico, Thomas, Torres, Barbara, Fang, Ping, Cheung, Sau Wai, Song, Xiaofei, Davis‐Williams, Angelique, Jornlin, Carly, Wight, Patricia A., Patyal, Pankaj, Taube, Jennifer, Poretti, Andrea, Inoue, Ken, Zhang, Feng, Pehlivan, Davut, Carvalho, Claudia M. B., Hobson, Grace M., Lupski, James R.
Published in Human mutation (01.01.2020)
Published in Human mutation (01.01.2020)
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Inside Back Cover, Volume 41, Issue 1
Hijazi, Hadia, Coelho, Fernanda S., Gonzaga‐Jauregui, Claudia, Bernardini, Laura, Mar, Soe S., Manning, Melanie A., Hanson‐Kahn, Andrea, Naidu, SakkuBai, Srivastava, Siddharth, Lee, Jennifer A., Jones, Julie R., Friez, Michael J., Alberico, Thomas, Torres, Barbara, Fang, Ping, Cheung, Sau Wai, Song, Xiaofei, Davis‐Williams, Angelique, Jornlin, Carly, Wight, Patricia A., Patyal, Pankaj, Taube, Jennifer, Poretti, Andrea, Inoue, Ken, Zhang, Feng, Pehlivan, Davut, Carvalho, Claudia M. B., Hobson, Grace M., Lupski, James R.
Published in Human mutation (01.01.2020)
Published in Human mutation (01.01.2020)
Get full text
Journal Article