Perinatal findings in a patient with a novel large chromosome 19p deletion

Clinical Case Reports
Marko CuljatJulia Timofeev

Abstract

We describe the prenatal and postnatal course of an infant with a large 19p deletion. Cases such as ours will improve the knowledge of specific gene functions for every medical specialist. The goal is to allow for a more rapid diagnosis, accurate prognosis and to decrease the likelihood of complications.

References

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