Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome (Q56372618)
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Current Data About Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome
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(P1476) "Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome" (language: en)
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(P2093) L J Wong
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T J Chen
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P Dai
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M Muenke
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(P356) 10.1002/AJMG.1461
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