Analysis of common SHOX gene sequence variants and ~4.9-kb PAR1 deletion in ISS patients.

J Genet

Faculty of Science, Departement of Anthropology and Human Genetics, Charles University in Prague, Vinicna 7, Prague 2, 128 43, Czech Republic.

Published: August 2014

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Source
http://dx.doi.org/10.1007/s12041-014-0375-yDOI Listing

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