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Whole Exon Deletion in the GFAP Gene Is a Novel Molecular Mechanism Causing Alexander Disease. [electronic resource] by
- Green, Lydia
- Berry, Ian R
- Childs, Anne-Marie
- McCullagh, Helen
- Jose, Sandhya
- Warren, Dan
- Craven, Ian
- Camm, Nick
- Prescott, Katrina
- van der Knaap, Marjo S
- Sheridan, Eamonn
- Livingston, John H
Producer: 20190913
In:
Neuropediatrics vol. 49
Availability: No items available.
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11.
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Cerebral hypomyelination associated with biallelic variants of FIG4. [electronic resource] by
- 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
- Skibina, Olga
- Ruddle, Jonathan
- Tan, Tiong Y
- Leventer, Richard J
- Livingston, John H
- Meisler, Miriam H
Producer: 20200309
In:
Human mutation vol. 40
Availability: No items available.
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