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Medical Journal of Australia, ISSN 0025-729X, 08/2015, Volume 203, Issue 3, pp. 132 - 133
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2016, Volume 374, Issue 25, pp. 2441 - 2452
Journal Article
npj Genomic Medicine, ISSN 2056-7944, 12/2017, Volume 2, Issue 1, pp. 16 - 9
Organisations and governments seeking to implement genomics into clinical practice face numerous challenges across multiple, diverse aspects of the health care... 
IMPLEMENTATION | GENETICS | INFANTS | GENETICS & HEREDITY | Medicine | Health care industry | Genomics
Journal Article
PLoS Medicine, ISSN 1549-1277, 08/2018, Volume 15, Issue 8, p. e1002630
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2008, Volume 9, Issue 5, pp. 462 - 472
Summary As the molecular basis of disease continues to be elucidated, familial cancer syndromes, which consist of a range of neoplastic and non-neoplastic... 
Hematology, Oncology and Palliative Medicine | COWDEN-SYNDROME | CELL CARCINOMA SYNDROME | GENOTYPE-PHENOTYPE CORRELATIONS | ONCOLOGY | NONPOLYPOSIS COLORECTAL-CANCER | MUIR-TORRE-SYNDROME | TUBEROUS-SCLEROSIS-COMPLEX | PEUTZ-JEGHERS-SYNDROME | HOGG-DUBE-SYNDROME | MULTIPLE ENDOCRINE NEOPLASIA | GORLIN-SYNDROME | Colonic Neoplasms - genetics | Kidney Neoplasms - genetics | Neoplastic Syndromes, Hereditary - pathology | Endocrine Gland Neoplasms - genetics | Genetic Testing | Peutz-Jeghers Syndrome - pathology | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Gene Expression Regulation, Neoplastic | Multiple Endocrine Neoplasia Type 2a - pathology | Adenomatous Polyposis Coli - pathology | Multiple Endocrine Neoplasia Type 2b - pathology | Tuberous Sclerosis - pathology | Basal Cell Nevus Syndrome - pathology | Leiomyomatosis - pathology | Neoplastic Syndromes, Hereditary - genetics | Skin - pathology | Skin Neoplasms - pathology | Hamartoma Syndrome, Multiple - pathology | Carcinoma, Renal Cell - pathology | Disease Progression | Neurofibromatosis 2 - pathology | Neurofibromatosis 1 - pathology | Endocrine Gland Neoplasms - pathology | Pedigree | Colonic Neoplasms - pathology | Skin Neoplasms - genetics | Kidney Neoplasms - pathology | Mutation | Multiple Endocrine Neoplasia - pathology | Genetic aspects | Skin | Colon cancer
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 03/2012, Volume 30, Issue 9, pp. 958 - 964
Journal Article
Medical Journal of Australia, ISSN 0025-729X, 11/2012, Volume 197, Issue 9, pp. 480 - 481
Journal Article
Public Health Genomics, ISSN 1662-4246, 2019, Volume 22, Issue 3-4, pp. 140 - 144
Journal Article
Australasian Journal of Dermatology, ISSN 0004-8380, 08/2019, Volume 60, Issue 3, pp. e245 - e246
Journal Article
Internal Medicine Journal, ISSN 1444-0903, 11/2018, Volume 48, Issue 11, pp. 1325 - 1330
Journal Article
Australasian Journal of Dermatology, ISSN 0004-8380, 05/2019, Volume 60, Issue 2, pp. e160 - e162
Journal Article
Gut, ISSN 0017-5749, 07/2011, Volume 60, Issue 7, pp. 950 - 957
Journal Article
Psychology & Health, ISSN 0887-0446, 10/2019, Volume 34, Issue 10, pp. 1141 - 1160
Objective: Hereditary Haemorrhagic Telangiectasia (HHT) is a genetic condition causing frequent nose bleeds, skin lesions (telangiectasia) and arteriovenous... 
genetic | stigma | psychological | Hereditary Haemorrhagic Telangiectasia | HHT | qualitative | narrative analysis | coping | POPULATION | INTEGRATED CARE PROGRAMS | PREVALENCE | EXPERIENCES | PSYCHOLOGY, MULTIDISCIPLINARY | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | EPISTAXIS | DISEASE | QUALITY-OF-LIFE | VALIDITY | NEUROFIBROMATOSIS TYPE-1 | SEVERITY
Journal Article
National Cancer Institute. Journal (Print), ISSN 0027-8874, 02/2010, Volume 102, Issue 3, pp. 193 - 201
Journal Article