Publication | Closed Access
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
466
Citations
9
References
2006
Year
Genetic DisorderGeneticsCommon Inversion PolymorphismHuman PolymorphismPathologyMolecular GeneticsGenomicsMedicineChromosome 9New Chromosome 17Q21.31Microdeletion SyndromeClinical Genetics
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