C. Freemantle

Sudden infant death syndrome and unascertainable deaths: Trends and disparities among Aboriginal and non‐Aboriginal infants born in Western Australia from 1980 to 2001 inclusive

F. Stanley, N. de Klerk, D. McAullay, 2006, Journal of paediatrics and child health.

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

E. Haan, D. Callen, H. Eyre, 1990, American journal of human genetics.

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

E. Haan, D. Callen, C. Freemantle, 1990, Journal of medical genetics.

Assignment of the gene for central core disease to chromosome 19

K. Friend, E. Haan, J. Mulley, 1990, Human Genetics.

Interpretation of recent sudden infant death syndrome rates in Western Australia

F. Stanley, N. de Klerk, A. Charles, 2005, Journal of paediatrics and child health.

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

E. Haan, D. Callen, H. Eyre, 1991, American journal of human genetics.

Indicators of infant and childhood mortality for indigenous and non-indigenous infants and children born in Western Australia from 1980 to 1997 inclusive

C. Freemantle, 2003 .

Patterns, trends, and increasing disparities in mortality for Aboriginal and non-Aboriginal infants born in Western Australia, 1980–2001: population database study

F. Stanley, N. Klerk, D. McAullay, 2006, The Lancet.