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Author/Creator McWalter, K.

1. Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy. Issue 4 (2nd August 2020)

Authors:
Robinson, H.K.; Zaklyazminskaya, E.; Povolotskaya, I.; Surikova, Y.; Mallin, L.; Armstrong, C.; Mabin, D.; Benke, P.J.; Chrisant, M.R.; McDonald, M.; Marboe, C.C.; Agre, K.E.; Deyle, D.R.; McWalter, K.; Douglas, G.; Balashova, M.S.; Kaimonov, V.; Shirokova, N.; Pomerantseva, E.; Turner, C.L.
Journal:
Clinical genetics
Issue:
Volume 98:Issue 4(2020)
Page Start:
331
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance. Issue 4 (7th January 2018)

Authors:
Powis, Z.; Farwell Hagman, K.D.; Mroske, C.; McWalter, K.; Cohen, J.S.; Colombo, R.; Serretti, A.; Fatemi, A.; David, K.L.; Reynolds, J.; Immken, L.; Nagakura, H.; Cunniff, C.M.; Payne, K.; Barbaro‐Dieber, T.; Gripp, K.W.; Baker, L.; Stamper, T.; Aleck, K.A.; Jordan, E.S.
Journal:
Clinical genetics
Issue:
Volume 93:Issue 4(2018)
Page Start:
752
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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