Ponnila S Marinescu

We don’t have enough information about this author to calculate their statistics. If you think this is an error let us know.
Learn More
We present the prenatal case of a 12.5-Mb duplication involving 6q25-qter and a 12.2-Mb deletion encompassing 10q26-qter diagnosed by aCGH, while conventional karyotype showed normal results. The genotype-phenotype correlation between individual microarray and clinical findings adds to the emerging atlas of chromosomal abnormalities associated with specific(More)
  • 1