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Author/Creator Huet, F

2. Clinical, molecular, and genotype–phenotype correlation studies from 25 cases of oral–facial–digital syndrome type 1: a French and Belgian collaborative study. Issue 1 (5th January 2006)

Authors:
Thauvin-Robinet, C; Cossée, M; Cormier-Daire, V; Van Maldergem, L; Toutain, A; Alembik, Y; Bieth, E; Layet, V; Parent, P; David, A; Goldenberg, A; Mortier, G; Héron, D; Sagot, P; Bouvier, A M; Huet, F; Cusin, V; Donzel, A; Devys, D; Teyssier, J R
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 1(2006)
Page Start:
54
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy. Issue 10 (1st October 2002)

Authors:
Van Maldergem, L; Magré, J; Khallouf, T E; Gedde-Dahl, T; Delépine, M; Trygstad, O; Seemanova, E; Stephenson, T; Albott, C S; Bonnici, F; Panz, V R; Medina, J-L; Bogalho, P; Huet, F; Savasta, S; Verloes, A; Robert, J-J; Loret, H; de Kerdanet, M; Tubiana-Rufi, N
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 10(2002)
Page Start:
722
Record Type:
Journal Article
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8. Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability. (18th March 2013)

Authors:
Callier, P; Aral, B; Hanna, N; Lambert, S; Dindy, H; Ragon, C; Payet, M; Collod‐Beroud, G; Carmignac, V; Delrue, MA; Goizet, C; Philip, N; Busa, T; Dulac, Y; Missotte, I; Sznajer, Y; Toutain, A; Francannet, C; Megarbane, A; Julia, S
Journal:
Clinical genetics
Issue:
Volume 84:Number 6(2013:Dec.)
Page Start:
507
Record Type:
Journal Article
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9. Temporary assist devices in France 2014–2018: intra-aortic balloon pump: is the technique really outdated?. (25th November 2020)

Authors:
Roubille, F; Akodad, M; Delmas, C; Bonnefoy-Cudraz, E; Huet, F; Leclercq, F; Gaudard, P; Rouviere, P; Gandet, T; Duflos, C; Delseny, D; Battistella, P; Agullo, A; Aguilhon, S; Puymirat, E
Journal:
European heart journal
Issue:
Volume 41:(2020)Supplement 2
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

10. The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening. Issue 11 (29th June 2009)

Authors:
Thauvin-Robinet, C; Munck, A; Huet, F; Génin, E; Bellis, G; Gautier, E; Audrézet, M-P; Férec, C; Lalau, G; Georges, M Des; Claustres, M; Bienvenu, T; Gérard, B; Boisseau, P; Cabet-Bey, F; Feldmann, D; Clavel, C; Bieth, E; Iron, A; Simon-Bouy, B
Journal:
Journal of medical genetics
Issue:
Volume 46:Issue 11(2009)
Page Start:
752
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗