Table 2. Complementation tests of proximal X-chromosome deficiencies.
Deficiency mapped |
|||||||
---|---|---|---|---|---|---|---|
Deficiency tested | Df(1)BSC708 | Df(1)LB6 | Df(1)54 | Df(1)Exel6255 | Df(1)DCB1-35c | Df(1)DCB1-35b | Df(1)R8A |
Df(1)BSC708 | − | − | − | − | − | − | + |
Df(1)LB6 | − | − | − | + | − | + | |
Df(1)54 | − | − | − | − | + | ||
Df(1)Exel6255 | − | − | − | + | |||
Df(1)DCB1-35c | − | − | + | ||||
Df(1)DCB1-35b | − | − | |||||
Df(1)R8A | − |
“−” indicates that the heteroallelic combination was lethal; “+” indicates that the combination was viable.