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Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect. [electronic resource] by
- Brouillard, P
- Ghassibé, M
- Penington, A
- Boon, L M
- Dompmartin, A
- Temple, I K
- Cordisco, M
- Adams, D
- Piette, F
- Harper, J I
- Syed, S
- Boralevi, F
- Taïeb, A
- Danda, S
- Baselga, E
- Enjolras, O
- Mulliken, J B
- Vikkula, M
Producer: 20060420
In:
Journal of medical genetics vol. 42
Availability: No items available.
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IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign. [electronic resource] by
- Desmyter, L
- Ghassibe, M
- Revencu, N
- Boute, O
- Lees, M
- François, G
- Verellen-Dumoulin, C
- Sznajer, Y
- Moncla, A
- Benateau, H
- Claes, K
- Devriendt, K
- Mathieu, M
- Van Maldergem, L
- Addor, M-C
- Drouin-Garraud, V
- Mortier, G
- Bouma, M
- Dieux-Coeslier, A
- Genevieve, D
- Goldenberg, A
- Gozu, A
- Makrythanasis, P
- McEntagart, U
- Sanchez, A
- Vilain, C
- Vermeer, S
- Connell, F
- Verheij, J
- Manouvrier, S
- Pierquin, G
- Odent, S
- Holder-Espinasse, M
- Vincent-Delorme, C
- Gillerot, Y
- Vanwijck, R
- Bayet, B
- Vikkula, M
Publication details: Molecular syndromology 2010
In:
Molecular syndromology vol. 1
Availability: No items available.
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