| Number | Title |
|---|
| 1 |
AN INTRODUCTION TO 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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