Related references
Note: Only part of the references are listed.Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus
James E. Self et al.
ARCHIVES OF OPHTHALMOLOGY (2007)
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Patrick Tarpey et al.
NATURE GENETICS (2006)
PRUNE and NM23-M1 expression in embryonic and adult mouse brain
Pietro Carotenuto et al.
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES (2006)
Molecular diversity of voltage-gated sodium channel α and β subunit mRNAs in human tissues
Luz Candenas et al.
EUROPEAN JOURNAL OF PHARMACOLOGY (2006)
Gene expression profiling during the embryonic development of mouse brain using an oligonucleotide-based microarray system
T Matsuki et al.
MOLECULAR BRAIN RESEARCH (2005)
Sex differences in sex chromosome gene expression in mouse brain
J Xu et al.
HUMAN MOLECULAR GENETICS (2002)
Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes
Jo Vandesompele et al.
GENOME BIOLOGY (2002)
Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays
SA Bustin
JOURNAL OF MOLECULAR ENDOCRINOLOGY (2000)
Share Paper
