Eléments de l'association
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List of bibliographic references
Number of relevant bibliographic references: 8.| Ident. | Authors (with country if any) | Title |
|---|---|---|
| 003A34 | Fc Connell [Royaume-Uni] ; K. Gordon [Royaume-Uni] ; G. Brice [Royaume-Uni] ; V. Keeley [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; P. Ostergaard [Royaume-Uni] | The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings |
| 003C43 | G. Brice [Royaume-Uni] ; P. Ostergaard ; S. Jeffery ; K. Gordon [Royaume-Uni] ; Ps Mortimer [Royaume-Uni] ; S. Mansour | A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family |
| 004832 | Fc Connell [Royaume-Uni] ; K. Kalidas ; P. Ostergaard ; G. Brice [Royaume-Uni] ; V. Murday [Royaume-Uni] ; Ps Mortimer ; I. Jeffrey [Royaume-Uni] ; S. Jeffery ; Sahar Mansour [Royaume-Uni] | CCBE1 mutations can cause a mild, atypical form of generalized lymphatic dysplasia but are not a common cause of non‐immune hydrops fetalis |
| 005274 | P. Ostergaard [Royaume-Uni] ; Ma Simpson [Royaume-Uni] ; S. Jeffery [Royaume-Uni] | Massively parallel sequencing and identification of genes for primary lymphoedema: a perfect fit |
| 006404 | F C Connell [Royaume-Uni] ; P. Ostergaard ; C. Carver ; G. Brice ; N. Williams ; S. Mansour ; Peter Mortimer (dermatologue) [Royaume-Uni] ; Steve Jeffery | Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas. |
| 006827 | F. C. Connell [Royaume-Uni] ; P. Ostergaard [Royaume-Uni] ; C. Carver [Royaume-Uni] ; G. Brice [Royaume-Uni] ; N. Williams [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; Peter Mortimer (dermatologue) [Royaume-Uni] ; Steve Jeffery [Royaume-Uni] | Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas |
| 007418 | C. Carver ; G. Brice ; S. Mansour ; P. Ostergaard ; Peter Mortimer (dermatologue) [Royaume-Uni] ; S. Jeffery | Three children with Milroy disease and de novo mutations in VEGFR3 |
| 007686 | S. Kumar [Arabie saoudite] ; C. Carver ; S. Mccall ; G. Brice ; P. Ostergaard ; Peter Mortimer (dermatologue) [Royaume-Uni] ; S. Jeffery [Royaume-Uni] | A family with lymphoedema‐distichiasis where identical twins have a discordant phenotype |
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