Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome

D Bevsen; J Raes; BP Leroy; A Lucassen; JR Yates; J Clayton-Smith; H Ilyna; SS Brooks; S Christin-Maitre; M Fellous; JP Fryns; JR Kim; P Lapunzina; E Lemyre; F Meire; LM Messiaen; Christine Oley; M Splitt; J Thomson; Y Van de Peer; RA Veitia; A De Paepe; E De Baere

Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome

D Bevsen, J Raes, BP Leroy, A Lucassen, JR Yates, J Clayton-Smith, H Ilyna, SS Brooks, S Christin-Maitre, M Fellous, JP Fryns, JR Kim, P Lapunzina, E Lemyre, F Meire, LM Messiaen, Christine Oley, M Splitt, J Thomson, Y Van de PeerRA Veitia, A De Paepe, E De Baere

Birmingham Medical School

Research output: Contribution to journal › Article

108 Citations (Scopus)

Original language	English
Pages (from-to)	205-218
Number of pages	14
Journal	American Journal of Human Genetics
Volume	72
Issue number	2
Publication status	Published - 1 Jan 2005

Cite this

Bevsen, D., Raes, J., Leroy, BP., Lucassen, A., Yates, JR., Clayton-Smith, J., Ilyna, H., Brooks, SS., Christin-Maitre, S., Fellous, M., Fryns, JP., Kim, JR., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, LM., Oley, C., Splitt, M., Thomson, J., ... De Baere, E. (2005). Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome. American Journal of Human Genetics, 72(2), 205-218.

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author = "D Bevsen and J Raes and BP Leroy and A Lucassen and JR Yates and J Clayton-Smith and H Ilyna and SS Brooks and S Christin-Maitre and M Fellous and JP Fryns and JR Kim and P Lapunzina and E Lemyre and F Meire and LM Messiaen and Christine Oley and M Splitt and J Thomson and {Van de Peer}, Y and RA Veitia and {De Paepe}, A and {De Baere}, E",

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Bevsen, D, Raes, J, Leroy, BP, Lucassen, A, Yates, JR, Clayton-Smith, J, Ilyna, H, Brooks, SS, Christin-Maitre, S, Fellous, M, Fryns, JP, Kim, JR, Lapunzina, P, Lemyre, E, Meire, F, Messiaen, LM, Oley, C, Splitt, M, Thomson, J, Van de Peer, Y, Veitia, RA, De Paepe, A & De Baere, E 2005, 'Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome', American Journal of Human Genetics, vol. 72, no. 2, pp. 205-218.

TY - JOUR

T1 - Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome

AU - Bevsen, D

AU - Raes, J

AU - Leroy, BP

AU - Lucassen, A

AU - Yates, JR

AU - Clayton-Smith, J

AU - Ilyna, H

AU - Brooks, SS

AU - Christin-Maitre, S

AU - Fellous, M

AU - Fryns, JP

AU - Kim, JR

AU - Lapunzina, P

AU - Lemyre, E

AU - Meire, F

AU - Messiaen, LM

AU - Oley, Christine

AU - Splitt, M

AU - Thomson, J

AU - Van de Peer, Y

AU - Veitia, RA

AU - De Paepe, A

AU - De Baere, E

PY - 2005/1/1

Y1 - 2005/1/1

M3 - Article

VL - 72

SP - 205

EP - 218

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 2

ER -