Screening for carriers of genetic disease : points to considerHAAN, E. A.Medical journal of Australia. 1993, Vol 158, Num 6, pp 419-421, issn 0025-729XArticle

Fetal exposure to herpesviruses may be associated with pregnancy-induced hypertensive disorders and preterm birth in a Caucasian populationGIBSON, C. S; GOLDWATER, P. N; MACLENNAN, A. H et al.BJOG (Oxford. Print). 2008, Vol 115, Num 4, pp 492-500, issn 1470-0328, 9 p.Article

Analysis of five Duchenne muscular dystrophy exons and gender determination using conventional duplex polymerase chain reaction on single cellsHUSSEY, N. D; HU DONGGUI; FROILAND, D. A. H et al.Molecular human reproduction. 1999, Vol 5, Num 11, pp 1089-1094, issn 1360-9947Article

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndromeFANG, Y.-Y; BAIN, S; HAAN, E. A et al.American journal of medical genetics. 1997, Vol 71, Num 4, pp 453-457, issn 0148-7299Article

Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiencyHAAN, E. A; SERJEANTSON, S. W; NORMAN, R et al.Medical journal of Australia. 1992, Vol 156, Num 2, pp 132-135, issn 0025-729XArticle

Assignment of the gene for central core disease to chromosome 19HAAN, E. A; FREEMANTLE, C. J; MCCURE, J. A et al.Human genetics. 1990, Vol 86, Num 2, pp 187-190, issn 0340-6717Article

Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduriaHAAN, E. A; SCHOLEM, R. D; PITT, J. J et al.European journal of pediatrics. 1987, Vol 146, Num 5, pp 484-488, issn 0340-6199Article

Molecular biology of phenylalanine hydroxylaseCOTTON, R. G. F; DAHL, H. H. M; MERCER, J. F. B et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 206-208, issn 0141-8955, suppl. 2Conference Paper

PEHO and PEHO-like syndromes: Report of five Australian casesFIELD, M. J; GRATTAN-SMITH, P; PIPER, S. M et al.American journal of medical genetics. 2003, Vol 122A, Num 1, pp 6-12, issn 0148-7299, 7 p.Article

Origins of accessory small ring marker chromosomes derived from chromosome 1CALLEN, D. F; EYRE, H; FANG, Y.-Y et al.Journal of medical genetics. 1999, Vol 36, Num 11, pp 847-853, issn 0022-2593Article

Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS) : implications for mapping and cloning the BOR geneGU, J. Z; WAGNER, M. J; HAAN, E. A et al.Genomics (San Diego, Calif.). 1996, Vol 31, Num 2, pp 201-206, issn 0888-7543Article

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndromeADES, L. C; MORRIS, L. L; POWER, R. G et al.American journal of medical genetics. 1995, Vol 57, Num 4, pp 565-572, issn 0148-7299Article

The sensitivity of ultrasound and serum alpha-fetoprotein in population-based antenatal screening for neural tube defects, South Australia 1986-1991CHAN, A; ROBERTSON, E. F; HAAN, E. A et al.British journal of obstetrics and gynaecology (Print). 1995, Vol 102, Num 5, pp 370-376, issn 0306-5456Article

Neurological involvement in worth type endosteal hyperostosis : report of a familyADES, L. C; MORRIS, L. L; BURNS, R et al.American journal of medical genetics. 1994, Vol 51, Num 1, pp 46-50, issn 0148-7299Article

Polydactyly, campomelia, ambiguous, genitalia, cystic dysplastic kidneys, and cerebral malformation in a fetus of consanguineous parents : a new multiple malformation syndrome, or a severe form of oral-facial digital syndrome type IV ?ADES, L. C; CLAPTON, W. K; MORPHETT, A et al.American journal of medical genetics. 1994, Vol 49, Num 2, pp 211-217, issn 0148-7299Article

Congenital heart malformation in Yunis-Varón syndromeADES, L. C; MORRIS, L. L; RICHARDSON, M et al.Journal of medical genetics. 1993, Vol 30, Num 9, pp 788-792, issn 0022-2593Article

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomesCALLEN, D. F; EYRE, H; YIP, M.-Y et al.American journal of medical genetics. 1992, Vol 43, Num 4, pp 709-715, issn 0148-7299Article

Use of linkage data obtained in single families : prenatal diagnosis of a new X-linked mental retardation syndromeMULLEY, J. C; GEDEON, A. K; WILSON, S et al.American journal of medical genetics. 1992, Vol 43, Num 1-2, pp 415-419, issn 0148-7299Article

Chromosomal origin of small ring marker chromosomes in man : characterization by molecular geneticsCALLEN, D. F; EYRE, H. J; RINGENBERGS, M. L et al.American journal of human genetics. 1991, Vol 48, Num 4, pp 769-782, issn 0002-9297Article

Predictive diagnosis for polycystic kidney disease using DNA markersMULLEY, J. C; HAAN, E. A; GEDEON, A. K et al.Medical journal of Australia. 1990, Vol 152, Num 6, pp 287-289, issn 0025-729XArticle

Succinic semialdehyde dehydrogenase deficiency: a further caseHAAN, E. A; BROWN, G. K; MITCHELL, D et al.Journal of inherited metabolic disease. 1985, Vol 8, Num 3, issn 0141-8955, 99Article

Biochemical evidence of selective nerve cell changes in the normal ageing human and rat brainALLEN, S. J; BENTON, J. S; GOODHARDT, M. J et al.Journal of neurochemistry. 1983, Vol 41, Num 1, pp 256-265, issn 0022-3042Article

Deoxyribose-5-phosphate aldolase deficiency―a harmless inborn error of metabolismCHAPPEL, A; SCHOLEM, R. D; BROWN, G. K et al.Journal of inherited metabolic disease. 1983, Vol 6, Num 3, pp 105-107, issn 0141-8955Article

The genomic basis of cerebral palsy: a HuGE systematic literature reviewO'CALLAGHAN, M. E; MACLENNAN, A. H; HAAN, E. A et al.Human genetics. 2009, Vol 126, Num 1, pp 149-172, issn 0340-6717, 24 p.Article

The impact of rubella immunisation on the incidence of rubella, congenital rubella syndrome and rubella-related terminations of pregnancy in South AustraliaCHEFFINS, T; CHAN, A; KEANE, R. J et al.British journal of obstetrics and gynaecology (Print). 1998, Vol 105, Num 9, pp 998-1004, issn 0306-5456Article