Citations for
1FRA16B
The rare human fragile site 16B.
Felbor U, Feichtinger W, Schmid M.
Cytogenet Genome Res 100(1-4):85-8. Review. 2003
2FRA16B
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat.
Yu S, Mangelsdorf M, Hewett D, Hobson L, Baker E, Eyre HJ, Lapsys N, Le Paslier D, Doggett NA, Sutherland GR, Richards RI.
Cell 88(3):367-74. 1997
3MT1@, FRA16B
Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1.
Kozman HM, et al.
Genomics 11 : 756-759. 1991
4FRA16B
A linkage group with FRA16B (the fragile site at 16q22.1).
Mulley JC, et al.
Hum Genet 82 : 131-133. 1989
5MT2A, FRA16A, FRA16B
Linkage analysis of markers near fragile sites on human chromosome 16.
Mulley JC, et al.
(HGM9) Cytogenet Cell Genet 46 : 665. 1987
6FRA16B
Fragile sites at 16q22 are not at the breakpoint of the chromosomal rearrangement in AMMoL.
Simmers RN, et al.
Science 236 : 92-94. 1987
7FRA16B, HP, HPR
The haptoglobin gene is distal to the fragile site at 16q22.
Simmers RN, et al.
(HGM8) Cytogenet Cell Genet 40 : 745. 1985
8FRA16B
Demonstration of a heritable fragile site in human chromosome 16 with distamycin A.
Schmid M, et al.
Cytogenet Cell Genet 28 : 87-94. 1980
9FRA16B, HP
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.
Magenis RE, et al.
Science 170 : 85-87. 1970