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Stark, Z, Gillam, L, Walker, SP, McGillivray, G.
Ethical controversies in prenatal microarray..
Curr Opin Obstet Gynecol
25(2)
:
133 -137
2013
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Stark, Z, Pangrazio, A, McGillivray, G, Fink, AM.
Association of severe autosomal recessive osteopetrosis and structural brain abnormalities: a case report and review of the literature..
Eur J Med Genet
56(1)
:
36 -38
2013
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Stark, Z, Gillessen-Kaesbach, G, Ryan, MM, Cirstea, IC, Gremer, L, Ahmadian, MR, Savarirayan, R, Zenker, M.
Two novel germline KRAS mutations: expanding the molecular and clinical phenotype..
Clin Genet
81(6)
:
590 -594
2012
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Bruno, DL, Stark, Z, Amor, DJ, Burgess, T, Butler, K, Corrie, S, Francis, D, Ganesamoorthy, D, Hills, L, James, PA, et al.
Extending the scope of diagnostic chromosome analysis: detection of single gene defects using high-resolution SNP microarrays..
Hum Mutat
32(12)
:
1500 -1506
2011
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Bruno, DL, White, SM, Ganesamoorthy, D, Burgess, T, Butler, K, Corrie, S, Francis, D, Hills, L, Prabhakara, K, Ngo, C, et al.
Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping..
J Med Genet
48(12)
:
831 -839
2011
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