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?
2013 ◽
Vol 120
(5)
◽
pp. 594-606
◽
2013 ◽
Vol 120
(10)
◽
pp. 1296-1296
◽
2013 ◽
Vol 120
(10)
◽
pp. 1297-1297
◽
2011 ◽
Vol 204
(1)
◽
pp. 26-38
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2016 ◽
Vol 20
(7)
◽
pp. 352-358
◽
2015 ◽
Vol 56
(6)
◽
pp. 4156
◽
2010 ◽
Vol 27
(2)
◽
pp. 193-198
◽
2014 ◽
Vol 207
(4)
◽
pp. 111-123
◽
2007 ◽
Vol 13
(16)
◽
pp. 4731-4739
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