— Centre for Genetics Education

Genetics Fact Sheets

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Number	Title
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

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