Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?
Moedjono, S.J.; Sparkes, R.S.
Annales de Genetique 23(4): 235-237
1980
ISSN/ISBN: 0003-3995 PMID: 6971603 Document Number: 161688
A female infant with multiple congenital anomalies was ascertained to have 46,XX,rec(18)dup q, inv(8)(p23q22) through a carrier father with pericentric inversion of chromosome 8 (46,XY,inv(8)(p23q22). Comparison of the clinical and cytogenetic findings are made with previously published similar cases.
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