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Author/Creator Wilson, Louise C.

11. Natural history and genotype‐phenotype correlations in 72 individuals with SATB2‐associated syndrome. Issue 4 (13th February 2018)

Authors:
Zarate, Yuri A.; Smith‐Hicks, Constance L.; Greene, Carol; Abbott, Mary‐Alice; Siu, Victoria M.; Calhoun, Amy R. U. L.; Pandya, Arti; Li, Chumei; Sellars, Elizabeth A.; Kaylor, Julie; Bosanko, Katherine; Kalsner, Louisa; Basinger, Alice; Slavotinek, Anne M.; Perry, Hazel; Saenz, Margarita; Szybow...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 4(2018)
Page Start:
925
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

12. Two further patients with the 1q24 deletion syndrome expand the phenotype: A possible role for the miR199–214 cluster in the skeletal features of the condition. (3rd September 2015)

Authors:
Ashraf, Tazeen; Collinson, Morag N.; Fairhurst, Joanna; Wang, Rubin; Wilson, Louise C.; Foulds, Nicola
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 12(2015:Dec.)
Page Start:
3153
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗