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About this Biochemistry, Genetics and Molecular Biology article

Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum by Cavalcanti, D. P.; Huber, C.; Le Quan Sang, K.-H.; Baujat, G.; Collins, F.; Delezoide, A.-L.; Dagoneau, N.; Le Merrer, M.; Martinovic, J.; Mello, M. F. S.; Vekemans, M.; Munnich, A.; Cormier-Daire, V. is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Cavalcanti, D. P.; Huber, C.; Le Quan Sang, K.-H.; Baujat, G.; Collins, F.; Delezoide, A.-L.; Dagoneau, N.; Le Merrer, M.; Martinovic, J.; Mello, M. F. S.; Vekemans, M.; Munnich, A.; Cormier-Daire, V.
Publisher
BMJ Publishing Group; BMJ (ISSN 0022-2593)
Published
2009
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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Browse all works by Cavalcanti, D. P.; Huber, C.; Le Quan Sang, K.-H.; Baujat, G.; Collins, F.; Delezoide, A.-L.; Dagoneau, N.; Le Merrer, M.; Martinovic, J.; Mello, M. F. S.; Vekemans, M.; Munnich, A.; Cormier-Daire, V.