Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis

Beysen, D; Fellous, MK; Fryns, Jean-Pierre; Splitt, M; Bouchard, P; Christin-Maitre, S; Veitia, R; Nygren, A; Schouten, J; Lemyre, E; Oley, C; Hjalgrim, H; Koivisto, PA; Messiaen, L; De Paepe, A; De Baerer, E

European Journal of Human Genetics

Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis

Author:

Beysen, D

Fellous, MK ; Fryns, Jean-Pierre ; Splitt, M ; Bouchard, P ; Christin-Maitre, S ; Veitia, R ; Nygren, A ; Schouten, J ; Lemyre, E ; Oley, C ; Hjalgrim, H ; Koivisto, PA ; Messiaen, L ; De Paepe, A ; De Baerer, E

Keywords:

0604 Genetics, 1103 Clinical Sciences, Genetics & Heredity, 3105 Genetics, 3202 Clinical sciences

European Journal of Human Genetics Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis

Author:

Keywords:

European Journal of Human Genetics

Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis