DNA analysis in patients with lissencephaly type I and other cortical dysplasias
- 1 September 1991
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 40 (3) , 383-386
- https://doi.org/10.1002/ajmg.1320400328
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Diagnostic Features And Clinical Signs Of 21 Patients With Lissencephaly Type IDevelopmental Medicine and Child Neurology, 1990
- Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1)American Journal of Medical Genetics, 1989
- Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.Journal of Medical Genetics, 1989
- Inverted neurons in agyriaHuman Genetics, 1986
- Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17American Journal of Medical Genetics, 1986
- Further comments on the lissencephaly syndromesAmerican Journal of Medical Genetics, 1985
- Syndromes with lissencephaly. I: Millerdieker and Norman‐Roberts syndromes and isolated lissencephalyAmerican Journal of Medical Genetics, 1984
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Miller-Dieker syndrome: Lissencephaly andmonosomy 17pThe Journal of Pediatrics, 1983
- An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?Journal of Medical Genetics, 1981