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Your search keyword '"Brouillard P"' showing total 5 results
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5 results on '"Brouillard P"'

1. Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery.

Author

UCL - SSS/DDUV/GEHU - Génétique, Witte, M H, Erickson, R P, Luy, L, Brouillard, P, Vikkula, M, UCL - SSS/DDUV/GEHU - Génétique, Witte, M H, Erickson, R P, Luy, L, Brouillard, P, and Vikkula, M

Abstract

We have created a human chromosomal map of the location of known and candidate genes involved in primary lymphedema (PLE). This should facilitate further discovery and provide a basis for understanding microdeletions which cause lymphedema.

Published
2021

2. Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery.

Author

UCL - SSS/DDUV/GEHU - Génétique, Witte, M H, Erickson, R P, Luy, L, Brouillard, P, Vikkula, M, UCL - SSS/DDUV/GEHU - Génétique, Witte, M H, Erickson, R P, Luy, L, Brouillard, P, and Vikkula, M

Abstract

We have created a human chromosomal map of the location of known and candidate genes involved in primary lymphedema (PLE). This should facilitate further discovery and provide a basis for understanding microdeletions which cause lymphedema.

Published
2021

3. Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

Author

Mendola, A., Schlogel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastre, E., Bygum, A., Vleuten, C.J. van der, Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M., Group, T.L.R., Mendola, A., Schlogel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastre, E., Bygum, A., Vleuten, C.J. van der, Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M., and Group, T.L.R.

Abstract

Item does not contain fulltext

Published
2013

4. Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

Author

Mendola, A., Schlogel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastre, E., Bygum, A., Vleuten, C.J. van der, Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M., Group, T.L.R., Mendola, A., Schlogel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastre, E., Bygum, A., Vleuten, C.J. van der, Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M., and Group, T.L.R.

Abstract

Item does not contain fulltext

Published
2013

5. Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

Author

Mendola, A., Schlogel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastre, E., Bygum, A., Vleuten, C.J. van der, Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M., Group, T.L.R., Mendola, A., Schlogel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastre, E., Bygum, A., Vleuten, C.J. van der, Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M., and Group, T.L.R.

Abstract

Item does not contain fulltext

Published
2013

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