Phenotype And NotFlorence Petit
List of bibliographic references
Number of relevant bibliographic references: 7.Ident. | Authors (with country if any) | Title |
---|---|---|
000021 | Francoise Pujol [Suède] ; Tina Hodgson [Suède] ; Ines Martinez-Corral [Suède] ; Anne-Catherine Prats [Suède] ; Danelle Devenport [Suède] ; Masatoshi Takeichi [Suède] ; Elisabeth Genot [Suède] ; Taija M Kinen [Suède] ; Philippa Francis-West [Suède] ; Barbara Garmy-Susini [Suède] ; Florence Tatin [France] | Dachsous1-Fat4 Signaling Controls Endothelial Cell Polarization During Lymphatic Valve Morphogenesis-Brief Report. |
000459 | Mylène Béri-Deixheimer [France] ; Marie-José Gregoire ; Annick Toutain ; Karène Brochet ; Sylvain Briault ; Jean-Luc Schaff ; Bruno Leheup ; Philippe Jonveaux | Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'. |
000660 | Inge D. C. Van Balkom ; Mariel Alders [Pays-Bas] ; Judith Allanson [Canada] ; Carlo Bellini [Italie] ; Ulrich Frank [Allemagne] ; Greetje De Jong [Afrique du Sud] ; Ingeborg Kolbe [Allemagne] ; Didier Lacombe [France] ; Stan Rockson [États-Unis] ; Peter Rowe [Canada] ; Frits Wijburg [Pays-Bas] ; Raoul C. M. Hennekam [Pays-Bas] | Lymphedema–lymphangiectasia–mental retardation (Hennekam) syndrome: A review |
000664 | M. Bahuau [France] ; C. Houdayer ; M. Tredano ; V. Soupre [France] ; R. Couderc ; M-P Vazquez [France] | FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate |
000756 | Sébastien Jacquemont [France] ; Sébastien Barbarot [France] ; Michelle Bocéno [France] ; Jean François Stalder [France] ; Albert David [France] | Familial congenital pulmonary lymphangectasia, non‐immune hydrops fetalis, facial and lower limb lymphedema: Confirmation of Njolstad's report |
000854 | C. Stoll [France] ; Y. Alembik [France] ; B. Dott [France] ; P. Kieffer [France] | Lymphedema combined with brachydactyly and tachycardia |
000A05 | D. Lacombe [France] ; A. Taieb ; P. Masson ; M. Fayon ; J L Demarquez | Neonatal Noonan syndrome with a molluscoid cutaneous excess over the scalp. |
This area was generated with Dilib version V0.6.31. |