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Ganesamoorthy, D, Bruno, D, McGillivray, G, Norris, F, White, S, Adroub, S, Amor, D, Yeung, A, Oertel, R, Pertile, et al.
Meeting the challenge of interpreting high‐resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?.
BJOG An International Journal of Obstetrics & Gynaecology
120(5)
:
594 -606
2013
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Turbitt, E, Amor, DJ, Halliday, JL, Metcalfe, SA.
Considerations for Reporting Genome Results to Patients.
Journal of Paediatrics and Child Health
49(1)
:
82 -82
2013
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Allou, L, Lambert, L, Amsallem, D, Bieth, E, Edery, P, Destrée, A, Rivier, F, Amor, D, Thompson, E, Nicholl, J, et al.
14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.
European Journal of Human Genetics
20(12)
:
1216 -1223
2012
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Brett, GR, Metcalfe, SA, Amor, DJ, Halliday, JL.
An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practice.
European Journal of Human Genetics
20(8)
:
825 -830
2012
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Loesch, DZ, Sherwell, S, Kinsella, G, Tassone, F, Taylor, A, Amor, D, Sung, S, Evans, A.
Fragile X‐associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene.
Clinical Genetics
82(1)
:
88 -92
2012
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