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NumberTitle
1 DNA, GENES AND CHROMOSOMES
2 VARIATIONS IN THE GENETIC CODE
3 GENE MUTATIONS
4 CHROMOSOME CHANGES
5 GENETIC CONDITIONS
6 GENETIC COUNSELLING
7 AUTOSOMAL RECESSIVE INHERITANCE
8 AUTOSOMAL DOMINANT INHERITANCE
9 X-LINKED RECESSIVE INHERITANCE
10 X-LINKED DOMINANT INHERITANCE
11 ENVIRONMENTAL AND GENETIC INTERACTIONS
12 MITOCHONDRIAL INHERITANCE
13 MOSAICISM
14 EPIGENETICS
15 GENETIC AND GENOMIC TESTING
16

CHROMOSOME MICROARRAY (CMA) TESTING IN CHILDREN & ADULTS   

Testing Guide: Chromosome Microarray (CMA) – Children and Adults
17 FORENSIC, PATERNITY AND ANCESTRY DNA TESTING
18 WHEN PARENTS ARE RELATED – CONSANGUINITY
19 ETHICAL ISSUES IN HUMAN GENETICS AND GENOMICS
20 LIFE INSURANCE PRODUCTS AND GENETIC TESTING IN AUSTRALIA
21 PHARMACOGENETICS / PHARMACOGENOMICS
22 CLONING AND STEM CELLS
23 GENE THERAPY
24

PRENATAL TESTING OVERVIEW

Booklet: Prenatal Testing: Special tests for your baby during pregnancy
25

SCREENING TESTS DURING PREGNANCY

Brochure: Screening Tests for Your Baby in Early Pregnancy 
26 DIAGNOSTIC TESTS DURING PREGNANCY
27 NON-INVASIVE PRENATAL TESTING (NIPT)
28 CHROMOSOME MICROARRAY (CMA) TESTING DURING PREGNANCY 
29 PREIMPLANTATION GENETIC DIAGNOSIS (PGD)
30 FOLATE BEFORE AND DURING EARLY PREGNANCY
31 CANCER AND GENETICS OVERVIEW
32 BREAST AND OVARIAN CANCER AND INHERITED PREDISPOSITION
33 BOWEL CANCER AND INHERITED PREDISPOSITION
34 GENETICS AND MELANOMA
35 GENETICS AND PROSTATE CANCER
36 TRISOMY 21 - DOWN SYNDROME
37 TRISOMY 13 - PATAU SYNDROME
38 TRISOMY 18 - EDWARDS SYNDROME
39 KLINEFELTER SYNDROME - XXY SYNDROME
40 TURNER SYNDROME - XO SYNDROME
41 CYSTIC FIBROSIS
42 TAY-SACHS DISEASE AND OTHER CONDITIONS MORE COMMON IN THE ASHKENAZI JEWISH COMMUNITY
43 THALASSAEMIA
44 SICKLE CELL DISEASE
45 NEUROFIBROMATOSIS TYPE 1
46 AUTISM SPECTRUM DISORDER
47 HEREDITARY HAEMOCHROMATOSIS
48 DIABETES TYPES 1 AND 2 AND INHERITED PREDISPOSITION
49 BLOOD  CLOTTING CONDITIONS (HEREDITARY THROMBOPHILIAS)
50 ALZHEIMER DISEASE
51 PARKINSON DISEASE
52 HAEMOPHILIA
53 DUCHENNE AND BECKER TYPES OF MUSCULAR DYSTROPHY
54 FRAGILE X SYNDROME
55

HUNTINGTON DISEASE

Booklet - Huntington Disease and Genetic Testing
56 FAMILIAL HYPERCHOLESTEROLAEMIA
57 CARDIOMYOPATHIES
58 PRIMARY ARRYTHMOGENIC DISORDERS
59 MENTAL ILLNESS - SCHIZOPHRENIA AND BIPOLAR DISORDER
60 NEURAL TUBE DEFECTS - SPINA BIFIDA AND ANENCEPHALY
61 TUBEROUS SCLEROSIS COMPLEX
62 NEUROFIBROMATOSIS TYPE 2
63 DEAFNESS AND HEARING LOSS
64 MTHFR GENE TESTING FOR PATIENTS
65 REPRODUCTIVE GENETIC CARRIER SCREENING

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