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Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing
UploadWNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome
UploadExpanding the spectrum of TBL1XR1 deletion: Report of a patient with brain and cardiac malformations
UploadPartial 1q Duplications and Associated Phenotype
Download from www.karger.comPartial Trisomy 17q and Partial Monosomy 20q in a Boy with Craniosynostosis
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