D. Chadwick

FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.

R. Weksberg, D. Chitayat, C. Shuman, 1996, American journal of medical genetics.

Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region.

F. Elmslie, A. Richens, M. Williamson, 1996, American journal of human genetics.

Molecular and cytogenetic characterization of a prenatally ascertained de novo (X;Y) translocation.

M. Speevak, S. Farrell, D. Chadwick, 2001, American journal of medical genetics.

Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

D. Curtis, F. Elmslie, C. Panayiotopoulos, 1997, Human molecular genetics.

Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13–14

D. Curtis, C. Panayiotopoulos, A. Arzimanoglou, 2002, Epilepsy Research.

RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

C L Bradshaw, L. Shaffer, C. Disteche, 1997, Prenatal diagnosis.