Open AccessRare human diseases: 9p deletion syndrome.
Author(s) -
В. О. Галаган
Publication year - 2014
Publication title -
medičnì perspektivi
Language(s) - Uncategorized
Resource type - Journals
eISSN - 2786-4804
pISSN - 2307-0404
DOI - 10.26641/2307-0404.2014.3.28507
Subject(s) - anamnesis , hypertelorism , palpebral fissure , proband , genetic counseling , karyotype , medicine , pediatrics , dermatology , pathology , genetics , biology , anatomy , chromosome , mutation , gene