Ada Hamosh MD, MPH, ‘Clinical Case Studies Illustrating Genetic Principles’ in Thompson & Thompson Genetics in Medicine (Elsevier, Eighth Edition, 2016) 394 <https://www-clinicalkey-com-au.ezp01.library.qut.edu.au/#!/content/book/3-s2.0-B9781437706963000200?scrollTo=%23sc0015>
Augui, Sandrine, Elphège P Nora and Edith Heard, ‘Regulation of X-Chromosome Inactivation by the X-Inactivation Centre’ (2011) 12(6) Nature Reviews Genetics 429
Bennett, Robin LFrench, Kathryn SteinhausResta, Robert GDoyle, Debra Lochner, ‘Standardized Human Pedigree Nomenclature: Update and Assessment of the Recommendations of the National Society of Genetic Counselors’ 17 Journal of Genetic Counseling 424 <https://www.proquest.com/docview/218649564?accountid=13380>
Boyd, JD and WJ Hamilton, ‘Foetus--or Fetus?’ (1967) 1(5537) BMJ 425
Brown, Carolyn JBallabio, Andreaet al, ‘A Gene from the Region of the Human X Inactivation Centre Is Expressed Exclusively from the Inactive X Chromosome’ 349(9) Nature 38 <https://www.proquest.com/docview/204459124?accountid=13380>
D. Peter Snustad , and Michael J. Simmons, ‘Chapter 15: Genomics (Chapter Portion)’ in Principles of Genetics (Wiley, 7th ed, 2015) 387 <https://ebookcentral.proquest.com/lib/qut/reader.action?docID=4806596&ppg=401>
D. Peter Snustad , and Michael J. Simmons, ‘Chapter 15: Genomics (Chapter Portion)’ in Principles of Genetics (Wiley, 7th ed, 2015) 387 <https://ebookcentral.proquest.com/lib/qut/reader.action?docID=4806596&ppg=401>
Disteche, Christine MBerletch, Joel B, ‘X-Chromosome Inactivation and Escape’ (2015) 94(4) Journal of Genetics 591 <https://www.proquest.com/docview/1754491907?accountid=13380>
Dobyns, William B et al, ‘Inheritance of Most X-Linked Traits Is Not Dominant or Recessive, Just X-Linked’ (2004) 129A(2) American Journal of Medical Genetics 136
Esteller, Manel, ‘Non-Coding RNAs in Human Disease’ 12 Nature Reviews. Genetics 861 <https://www.proquest.com/docview/905092976?accountid=13380>
Frenette, Paul SAtweh, George F, ‘Sickle Cell Disease: Old Discoveries, New Concepts, and Future Promise’ 117(7) 850 <https://www.proquest.com/docview/200538792?accountid=13380>
Hamamy, Hanan et al, ‘Consanguineous Marriages, Pearls and Perils: Geneva International Consanguinity Workshop Report’ (2011) 13(9) Genetics in Medicine 841
Harrow, J et al, ‘GENCODE: The Reference Human Genome Annotation for The ENCODE Project’ (2012) 22(9) Genome Research 1760
Houtgraaf, Jaco H, Jorie Versmissen and Wim J van der Giessen, ‘A Concise Review of DNA Damage Checkpoints and Repair in Mammalian Cells’ (2006) 7(3) Cardiovascular Revascularization Medicine 165
Jensen, Ole N, ‘Interpreting the Protein Language Using Proteomics’ 7(6) Nature Reviews. Molecular Cell Biology 391 <https://www.proquest.com/docview/224665544?accountid=13380>
Jesse D. Riordan and Joseph H. Nadeau, ‘From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health’ (2017) 101(2) American Journal of Human Genetics 177
Knudsen, Gun Peggy, ‘Gender Bias in Autoimmune Diseases’ (2009) 286(1–2) Journal of the Neurological Sciences 43
Korf, Bruce R and Mira B Irons, ‘The Human Genome’ in Human Genetics and Genomics (John Wiley and Sons Ltd, 4th Revised edition, 2013) 77
Lam, Jenny K WChow, Michael Y TZhang, YuLeung, Susan W S, ‘siRNA Versus miRNA as Therapeutics for Gene Silencing’ 4 Molecular Therapy. Nucleic Acids 745 <https://www.proquest.com/docview/1796352097?accountid=13380>
Lander, Eric S et al, ‘Initial Sequencing and Analysis of the Human Genome’ (2001) 409(6822) Nature 860
Maria Kousi and Nicholas Katsanis, ‘Genetic Modifiers and Oligogenic Inheritance’ (2015) 5(6 (Article 017145)) Cold Spring Harbor Perspectives in Medicine
Nussbaum, Robert, L., McInness, Roderick, R., and Willard, Huntinton, F., ‘Introduction to the Human Genome’ in Thompson & Thompson Genetics in Medicine (Elsevier, 8th ed, 2016) 3 <https://www.clinicalkey.com.au/#!/content/book/3-s2.0-B9781437706963000029>
Pan, Qun et al, ‘Deep Surveying of Alternative Splicing Complexity in the Human Transcriptome by High-Throughput Sequencing’ (2008) 40(12) Nature Genetics 1413
Pan, Qun et al, ‘Deep Surveying of Alternative Splicing Complexity in the Human Transcriptome by High-Throughput Sequencing’ (2008) 40(12) Nature Genetics 1413
Pink, RC et al, ‘Pseudogenes: Pseudo-Functional or Key Regulators in Health and Disease?’ (2011) 17(5) RNA 792
Qun Pan,Ofer Shai,Leo J. Lee,Brendan J. Frey,Benjamin J. Blencowe, ‘Deep Surveying of Alternative Splicing Complexity in the Human Transcriptome by High-Throughput Sequencing’ Nature Genetics <http://go.galegroup.com/ps/i.do?p=HRCA&u=qut&id=GALE|A192498260&v=2.1&it=r&sid=summon&authCount=1#>
Robert L. Nussbaum MD, FACP, FACMG, ‘Patterns of Single-Gene Inheritance’ in Thompson & Thompson Genetics in Medicine (Elsevier, 8th ed, 2016) 107 <https://www.clinicalkey.com.au/#!/content/book/3-s2.0-B9781437706963000078>
Robert L. Nussbaum MD, FACP, FACMG, ‘The Human Genome: Gene Structure and Function’ in Thompson & Thompson Genetics in Medicine (Elsevier, Eighth Edition, 2016) 21 <https://www-clinicalkey-com-au.ezp01.library.qut.edu.au/#!/content/book/3-s2.0-B9781437706963000030>
Rodenhiser, D, ‘Epigenetics and Human Disease: Translating Basic Biology into Clinical Applications’ (2006) 174(3) Canadian Medical Association Journal 341
Schoenwolf, Gary C et al, Larsen’s Human Embryology (at Fifth edition) <http://qut.alma.exlibrisgroup.com/view/action/uresolver.do?operation=resolveService&package_service_id=2724006090004001&institutionId=4001&customerId=4000>
Snustad, D Peter and Michael J Simmons, ‘Chapter 3: Mendelism: The Basic Principles of Inheritance’ in Principles of Genetics (Wiley, 7th ed, 2015) 40 <https://ebookcentral.proquest.com/lib/qut/reader.action?docID=4806596&ppg=62&c=UERG>
Snustad, D Peter and Michael J Simmons, ‘Chapter 4: Extensions of Mendelism’ in Principles of Genetics (Wiley, 7th ed, 2016) 62 <https://ebookcentral.proquest.com/lib/qut/reader.action?docID=4806596&ppg=84&c=UERG>
‘The ENCODE (ENCyclopedia Of DNA Elements) Project’ (2004) 306(5696) Science 636
