Authors:
Tiller, GE
Hannig, VL
Dozier, D
Carrel, L
Trevarthen, KC
Wilcox, WR
Mundlos, S
Haines, JL
Gedeon, AK
Gecz, J
Citation: Ge. Tiller et al., A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda, AM J HU GEN, 68(6), 2001, pp. 1398-1407
Citation: Dj. Wolff et al., Molecular determination of X inactivation pattern correlates with phenotype in women with a structurally abnormal X chromosome, GENET MED, 2(2), 2000, pp. 136-141
Authors:
Bailey, JA
Carrel, L
Chakravarti, A
Eichler, EE
Citation: Ja. Bailey et al., Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis, P NAS US, 97(12), 2000, pp. 6634-6639
Citation: L. Carrel et Hf. Willard, Heterogeneous gene expression from the inactive X chromosome: An X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others, P NAS US, 96(13), 1999, pp. 7364-7369
Citation: K. Mroz et al., Germ cell development in the XXY mouse: Evidence that X chromosome reactivation is independent of sexual differentiation, DEVELOP BIO, 207(1), 1999, pp. 229-238