Author/Creator: Witte, David P. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Witte, David P.

1. A novel pathogenic variant in OFD1 results in X‐linked Joubert syndrome with orofaciodigital features and pituitary aplasia. Issue 6 (20th March 2019)

Authors:: Aljeaid, Deema; Lombardo, Rachel C.; Witte, David P.; Hopkin, Robert J.
Journal:: American journal of medical genetics
Issue:: Volume 179:Issue 6(2019)
Page Start:: 1010
Record Type:: Journal Article
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2. Early-Lethal Costello Syndrome Due to Rare HRAS Tandem Base Substitution (c.35_36GC>AA; p.G12E)–Associated Pulmonary Vascular Disease. (November 2014)

Authors:: Weaver, K. Nicole; Wang, Dehua; Cnota, James; Gardner, Nicholas; Stabley, Deborah; Sol-Church, Katia; Gripp, Karen W.; Witte, David P.; Bove, Kevin E.; Hopkin, Robert J.
Journal:: Pediatric and developmental pathology
Issue:: Volume 17:Number 6(2014)
Page Start:: 421
Record Type:: Journal Article
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