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Beverley Bewes
Beverley Bewes
Genetics
Biology
Euchromatin
Gene duplication
Phenotype
4
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41
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Angelman Syndrome due to a Maternally Inherited Intragenic Deletion Encompassing Exons 7 and 8 of the UBE3A Gene
2017
Cytogenetic and Genome Research
Athina Ververi
Lily Islam
Beverley Bewes
Louise Busby
Caroline Sullivan
Natalie Canham
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16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2
2013
European Journal of Human Genetics
John C K Barber
V. Hall
Viv Maloney
Shuwen Huang
Angharad M Roberts
Angela F Brady
Nicki Foulds
Beverley Bewes
Marianne Volleth
Thomas Liehr
Karl Mehnert
Mark S. Bateman
Helen E. White
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16p11.2-p21.2 duplication syndrome differentiated from euchromatic variation of 16p11.2 in three new families
2012
John C K Barber
V. Hall
Viv Maloney
Beverley Bewes
K. MacDermot
S. Holder
Thomas Liehr
Marianne Volleth
Shuwen Huang
Helen E. White
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Deletions of 2q14 that include the homeobox engrailed 1 (EN1) transcription factor are compatible with a normal phenotype
2006
European Journal of Human Genetics
John C K Barber
Viv K. Maloney
Beverley Bewes
Emma L. Wakeling
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Citations (13)
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