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Fact Sheet Users Guide

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Title
AN INTRODUCTION TO DNA, GENES AND CHROMOSOMES
VARIATIONS IN THE GENETIC CODE
TYPES OF GENETIC VARIATION
CHROMOSOME CHANGES
GENETIC CONDITIONS
GENETIC COUNSELLING
AUTOSOMAL RECESSIVE INHERITANCE
AUTOSOMAL DOMINANT INHERITANCE
X-LINKED RECESSIVE INHERITANCE
X-LINKED DOMINANT INHERITANCE
ENVIRONMENTAL AND GENETIC INTERACTIONS
MITOCHONDRIAL INHERITANCE
MOSAICISM
EPIGENETICS

GENETIC AND GENOMIC TESTING

Personalised Medicine

CHROMOSOME MICROARRAY (CMA) TESTING IN CHILDREN & ADULTS   

Testing Guide: Chromosome Microarray (CMA) – Children and Adults

FORENSIC, PATERNITY AND ANCESTRY DNA TESTING
WHEN PARENTS ARE RELATED – CONSANGUINITY
ETHICAL ISSUES IN HUMAN GENETICS AND GENOMICS
LIFE INSURANCE PRODUCTS AND GENETIC TESTING IN AUSTRALIA
PHARMACOGENETICS AND PHARMACOGENOMICS
CLONING AND STEM CELLS

GENE THERAPY AND ADVANCED THERAPEUTICS

PRENATAL TESTING OVERVIEW

Booklet: Prenatal Testing: Special tests for your baby during pregnancy

SCREENING TESTS DURING PREGNANCY

Brochure: Screening Tests for Your Baby in Early Pregnancy 

DIAGNOSTIC TESTS DURING PREGNANCY
NON-INVASIVE PRENATAL TESTING (NIPT)
CHROMOSOME MICROARRAY (CMA) TESTING DURING PREGNANCY 
PREIMPLANTATION GENETIC DIAGNOSIS (PGD)

VITAMINS IN PREGNANCY

There are vitamins and minerals in pregnancy and breastfeeding that support a baby's development. These include folate and iodine.

CANCER GENETICS OVERVIEW
BREAST CANCER & INHERITED SUSCEPTIBILITY
BOWEL CANCER & INHERITED SUSCEPTIBILITY
MELANOMA & INHERITED SUSCEPTIBILITY
PROSTATE CANCER & INHERITED SUSCEPTIBILITY
TRISOMY 21 - DOWN SYNDROME
TRISOMY 13 - PATAU SYNDROME
TRISOMY 18 - EDWARDS SYNDROME
KLINEFELTER SYNDROME 
TURNER SYNDROME 
CYSTIC FIBROSIS
TAY-SACHS DISEASE AND OTHER CONDITIONS MORE COMMON IN THE ASHKENAZI JEWISH COMMUNITY
THALASSAEMIA
SICKLE CELL DISEASE
NEUROFIBROMATOSIS TYPE 1
AUTISM SPECTRUM DISORDER
HEREDITARY HAEMOCHROMATOSIS
DIABETES TYPES 1 AND 2 AND INHERITED PREDISPOSITION
BLOOD  CLOTTING CONDITIONS (HEREDITARY THROMBOPHILIAS)
ALZHEIMER DISEASE
PARKINSON DISEASE
HAEMOPHILIA
DUCHENNE AND BECKER TYPE MUSCULAR DYSTROPHY
FRAGILE X SYNDROME

HUNTINGTON DISEASE

Booklet - Huntington Disease and Genetic Testing

FAMILIAL HYPERCHOLESTEROLAEMIA
CARDIOMYOPATHIES
PRIMARY ARRYTHMOGENIC DISORDERS
MENTAL ILLNESS - SCHIZOPHRENIA AND BIPOLAR DISORDER
NEURAL TUBE DEFECTS - SPINA BIFIDA AND ANENCEPHALY
TUBEROUS SCLEROSIS COMPLEX
NEUROFIBROMATOSIS TYPE 2
DEAFNESS AND HEARING LOSS
MTHFR GENE TESTING FOR PATIENTS

REPRODUCTIVE GENETIC CARRIER SCREENING

GENETIC TESTING RESULTS

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Cancer in the family

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Intellectual Disability Genomic Testing