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+--- Thread: genetics 9 - kashmala (/showthread.php?tid=136137)
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genetics 9 - kashmala - ArchivalUser - 11-06-2006
A pregnant woman with a family history of fragile X
syndrome wants prenatal diagnosis of her fetus. Amplifica-
tion of the appropriate region of the FMRI gene by PCR is
attempted on DNA from amniotic fluid cells, but no ampli-
fied products are obtained. What is the best next step?
A Routine karyotype of the amniotic fluid cells
B Routine karyotype of the unaffected father
C Southern blot of the DNA from the anmiotic fluid
cells
D PCR analysis of the mother's FMR1 gene
E No further tests necessary
0 - ArchivalUser - 11-06-2006
e????
0 - ArchivalUser - 11-06-2006
e????
0 - ArchivalUser - 11-06-2006
southern blot of the dna ie ,C
0 - ArchivalUser - 11-06-2006
southern blot of the dna ie ,C
0 - ArchivalUser - 11-06-2006
southern blot of the dna ie ,C
0 - ArchivalUser - 11-06-2006
southern blot of the dna ie ,C
0 - ArchivalUser - 11-06-2006
EEEE
0 - ArchivalUser - 11-06-2006
EEEE
0 - ArchivalUser - 11-06-2006
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