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- Revencu, N (author)
Germline loss-of-function mutations in EPHB4 cause a second form of capillary malformation-arteriovenous malformation (CM-AVM2) deregulating RAS-MAPK signaling
- Article/chapterEnglish2019
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- 2019
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:142064558
- http://kipublications.ki.se/Default.aspx?queryparsed=id:142064558URI
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- Language:English
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- SwePubSwePub
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- Amyere, M (author)
- Helaers, R (author)
- Pairet, E (author)
- Baselga, E (author)
- Cordisco, M (author)
- Chung, W (author)
- Dubois, J (author)
- Lacour, J (author)
- Martorell, L (author)
- Mazereeuw-Hautier, J (author)
- Pyeritz, R (author)
- Amor, D (author)
- Bisdorff, A (author)
- Blei, F (author)
- Bombei, H (author)
- Dompmartin, A (author)
- Brooks, D (author)
- Dupont, J (author)
- Gonzalez-Ensenat, M (author)
- Frieden, I (author)
- Gerard, M (author)
- Kvarnung, M (author)
- Hanson-Kahn, AK (author)
- Hudgins, L (author)
- Leaute-Labreze, C (author)
- McCuaig, C (author)
- Metry, D (author)
- Parent, P (author)
- Paul, C (author)
- Petit, F (author)
- Phan, A (author)
- Quere, I (author)
- Salhi, A (author)
- Turner, A (author)
- Vabres, P (author)
- Vicente, A (author)
- Wargon, O (author)
- Watanabe, S (author)
- Weibel, L (author)
- Wilson, A (author)
- Willing, M (author)
- Mulliken, J (author)
- Boon, L (author)
- Vikkula, M (author)
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- In:EUROPEAN JOURNAL OF HUMAN GENETICS27, s. 844-8451018-4813
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- Vicente, A
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