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Author/Creator Berry, Ian R.

2. Cerebral hypomyelination associated with biallelic variants of FIG4. Issue 5 (28th February 2019)

Authors:
Lenk, Guy M.; Berry, Ian R.; Stutterd, Chloe A.; Blyth, Moira; Green, Lydia; Vadlamani, Gayatri; Warren, Daniel; Craven, Ian; Fanjul‐Fernandez, Miriam; Rodriguez‐Casero, Victoria; Lockhart, Paul J.; Vanderver, Adeline; Simons, Cas; Gibb, Susan; Sadedin, Simon; White, Susan M.; Christodoulou, John...
Journal:
Human mutation
Issue:
Volume 40:Issue 5(2019)
Page Start:
619
Record Type:
Journal Article
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3. Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20. Issue 5 (6th March 2021)

Authors:
Nikolopoulos, Georgios; Smith, Claire E. L.; Poulter, James A.; Murillo, Gina; Silva, Sandra; Lamb, Teresa; Berry, Ian R.; Brown, Catriona J.; Day, Peter F.; Soldani, Francesca; Al‐Bahlani, Suhaila; Harris, Sarah A.; O'Connell, Mary J.; Inglehearn, Chris F.; Mighell, Alan J.
Journal:
Human mutation
Issue:
Volume 42:Issue 5(2021)
Page Start:
567
Record Type:
Journal Article
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4. Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho‐dento‐osseous syndrome. (9th September 2018)

Authors:
Whitehouse, Laura L. E.; Smith, Claire E. L.; Poulter, James A.; Brown, Catriona J.; Patel, Anesha; Lamb, Teresa; Brown, Lucy R.; O'Sullivan, Elizabeth A.; Mitchell, Rowena E.; Berry, Ian R.; Charlton, Ruth; Inglehearn, Chris F.; Mighell, Alan J.
Journal:
Oral diseases
Issue:
Volume 25:Number 1(2019)
Page Start:
182
Record Type:
Journal Article
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