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Author/Creator Witte, Marlys

1. A five generation family with a novel mutation in FOXC2 and lymphedema worsening to hydrops in the youngest generation. Issue 11 (22nd September 2014)

Authors:
Sargent, Carole; Bauer, Julien; Khalil, Muhamed; Filmore, Parker; Bernas, Michael; Witte, Marlys; Pearson, M. Peggy; Erickson, Robert P
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 11(2014.)
Page Start:
2802
Record Type:
Journal Article
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2. Clinical heterogeneity in lymphoedema-distichiasis withFOXC2 truncating mutations. Issue 11 (1st November 2001)

Authors:
Erickson, Robert P; Dagenais, Susan L; Caulder, Mark S; Downs, Catherine A; Herman, Gail; Jones, Marilyn C; Kerstjens-Frederikse, Wilhelmina S; Lidral, Andrew C; McDonald, Marie; Nelson, Christine C; Witte, Marlys; Glover, Thomas W
Journal:
Journal of medical genetics
Issue:
Volume 38:Issue 11(2001)
Page Start:
761
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Downregulation of FoxC2 Increased Susceptibility to Experimental Colitis: Influence of Lymphatic Drainage Function?. Issue 6 (June 2015)

Authors:
Becker, Felix; Potepalov, Sergey; Shehzahdi, Romana; Bernas, Michael; Witte, Marlys; Abreo, Fleurette; Traylor, James; Orr, Wayne A.; Tsunoda, Ikuo; Alexander, Jonathan Steven
Journal:
Inflammatory bowel diseases
Issue:
Volume 21:Issue 6(2015:Jun.)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗