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Filters: Keyword is High-Throughput Nucleotide Sequencing and Author is Bongers, Ernie M H F [Clear All Filters]
De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. Am J Hum Genet. 2015 ;97(6):904-13.
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