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Downie, L, Halliday, JL, Burt, RA, Lunke, S, Lynch, E, Martyn, M, Poulakis, Z, Gaff, C, Sung, V, Wake, M, et al.
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort..
BMJ Paediatr Open
1(1)
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e000119
2017
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Bradford, D, Berkovsky, S, Martyn, M, Bakkar, T, Krahnert, M, Rodriguez, M, Bauer, D, Ireland, D, Gaff, C.
Interacting with Genomic Data: Clinician Requirements and Prototype Structure..
Stud Health Technol Inform
239:
1 -7
2017
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Cotter, M, Archibald, AD, McClaren, BJ, Burgess, T, Francis, D, Hills, L, Martyn, M, Oertel, R, Slater, H, Cohen, J, et al.
Clinical audit of genetic testing and referral patterns for fragile X and associated conditions..
Am J Med Genet A
170(6)
:
1439 -1449
2016
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Martyn, M, Anderson, V, Archibald, A, Carter, R, Cohen, J, Delatycki, M, Donath, S, Emery, J, Halliday, J, Hill, M, et al.
Offering fragile X syndrome carrier screening: a prospective mixed-methods observational study comparing carrier screening of pregnant and non-pregnant women in the general population..
BMJ Open
3(9)
:
e003660
2013
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Burke, S, Martyn, M, Thomas, H, Farndon, P.
The development of core learning outcomes relevant to clinical practice: identifying priority areas for genetics education for non-genetics specialist registrars..
Clin Med (Lond)
9(1)
:
49 -52
2009
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