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Search Results - Davis‐Williams, Angelique
Search Results - Davis‐Williams, Angelique
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Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome
by
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
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Inside Back Cover, Volume 41, Issue 1
by
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
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Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus–Merzbacher disease
by
Wolf, Nicole I.
,
Sistermans, Erik A.
,
Cundall, Maria
,
Hobson, Grace M.
,
Davis-Williams, Angelique P.
,
Palmer, Rodger
,
Stubbs, Paula
,
Davies, Sally
,
Endziniene, Milda
,
Wu, Yvonne
,
Chong, Wui K.
,
Malcolm, Sue
,
Surtees, Robert
,
Garbern, James Y.
,
Woodward, Karen J.
Published in
Brain (London, England : 1878)
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A large X-chromosomal deletion is associated with microphthalmia with linear skin defects (MLS) and amelogenesis imperfecta (XAI)
by
Hobson, Grace M.
,
Gibson, Carolyn W.
,
Aragon, Melissa
,
Yuan, Zhi-an
,
Davis-Williams, Angelique
,
Banser, Linda
,
Kirkham, Jennifer
,
Brook, Alan H.
Published in
American journal of medical genetics. Part A
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Variable Expression of a Novel PLP1 Mutation in Members of a Family With Pelizaeus-Merzbacher Disease
by
Fattal-Valevski, Aviva
,
DiMaio, Miriam S.
,
Hisama, Fuki M.
,
Hobson, Grace M.
,
Davis-Williams, Angelique
,
Garbern, James Y.
,
Mahoney, Maurice J.
,
Kolodny, Edwin H.
,
Pastores, Gregory M.
Published in
Journal of child neurology
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