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  1. ...of similarity to the arm regions ( Fig. 3B ), seen in seven large IRs ( Table 1 ). The internal IRs characteristic of patterns 1 and 2 ( Fig. 3, A and B , respectively) such as IRX-69.804 ( Fig. 3A ) were originally detected by IRF but excluded from the final set of 96 IRs because they contributed to secondary...
  2. .... 2019). The putative ancestral orientation and the original inversion event were defined based on the O1 and O2 haplotype diversity and the frequency and geographical distribution of haplotypes (normally taking as ancestral those found in African samples) (Supplemental Table S8). Additional independent...
  3. ....J. , Rider S.H. , Monaco A.P. , Eble B. , Schlessinger D. , Willard H.F. ( 1995 ) Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22. Hum. Mol. Genet. 4 : 731 – 739 . ↵ Minet M. , Grossenbacher-Grunder A.-M. , Thuriaux P. ( 1980 ) The origin...
  4. ...Bebber F. , Brobeta , Dekens M.P. , Finger K. , Fricke C. , Gates M.A. , Geiger H. , et al. ( 1999 ) A radiation hybrid map of the zebrafish . Nat. Genet. 23 : 86 – 89 . ↵ Holland P.W. , Garcia-Fernandez J. , Williams N.A. , Sidow A. ( 1994 ) Gene duplications and the origin of vertebrate development...
  5. ...-specific cosmid libraries originate from two different genomic sources, comparative Eco RI digests between these two sources served as an important check and balance in confirming the integrity of the genomic clones used in the construction of a physical map of this region. Two BAC/cosmid contigs were...
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