PT  - JOURNAL ARTICLE
AU  - Lavedan, C
AU  - Hofmann, H
AU  - Shelbourne, P
AU  - Duros, C
AU  - Savoy, D
AU  - Johnson, K
AU  - Junien, C
TI  - Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers.
AID  - 10.1136/jmg.28.2.89
DP  - 1991 Feb 01
TA  - Journal of Medical Genetics
PG  - 89--91
VI  - 28
IP  - 2
4099  - http://jmg.bmj.com/content/28/2/89.short
4100  - http://jmg.bmj.com/content/28/2/89.full
SO  - J Med Genet1991 Feb 01; 28
AB  - We report on two cases of prenatal diagnosis of myotonic dystrophy (DM), using flanking markers APOC2 or CKMM on the proximal side and D19S51 on the distal side. By double digestion (TaqI and NcoI) of PCR amplified CKMM, the informativeness was increased from a PIC value of 0.57 to 0.69. Altogether, with a PIC value of 0.64 for APOC2, 0.69 for CKMM, and 0.27 for D19S51 (BglI), presymptomatic and prenatal diagnosis can thus be offered to approximately 24% of persons with a risk between 0.0004 and 0.0008 using these flanking markers.