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

Author/Creator Brouillard, P.

1. Hypotrichosis‐lymphedema‐telangiectasia‐renal defect associated with a truncating mutation in the SOX18 gene. (16th April 2014)

Authors:: Moalem, S.; Brouillard, P.; Kuypers, D.; Legius, E.; Harvey, E.; Taylor, G.; Francois, M.; Vikkula, M.; Chitayat, D.
Journal:: Clinical genetics
Issue:: Volume 87:Number 4(2015:Apr.)
Page Start:: 378
Record Type:: Journal Article
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2. Predictors and impact of postoperative atrial fibrillation following thoracic surgery: a state‐of‐the‐art review. (11th January 2023)

Authors:: Diallo, E.‐H.; Brouillard, P.; Raymond, J.‐M.; Liberman, M.; Duceppe, E.; Potter, B. J.
Journal:: Anaesthesia
Issue:: Volume 78:Number 4(2023)
Page Start:: 491
Record Type:: Journal Article
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3. Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema. Issue 1 (15th March 2018)

Authors:: Fastré, E.; Lanteigne, L‐E.; Helaers, R.; Giacalone, G.; Revencu, N.; Dionyssiou, D.; Demiri, E.; Brouillard, P.; Vikkula, M.
Journal:: Clinical genetics
Issue:: Volume 94:Issue 1(2018)
Page Start:: 179
Record Type:: Journal Article
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