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You searched for: Date 2017 Journal Clinical case reports- 616.09 564
- Medicine -- Periodicals 564
- 10p monosomy -- chromosomal microarray -- GATA3 -- ZMYND11 1
- 12‐lead ECG -- lead extraction -- lead malposition -- ventricular tachycardia 1
- 16p11.2 deletion -- 16p11.2 duplication -- 16p11.2 triplication -- ASD risk variant -- gene triplication 1
- 18F‐FDG -- Hodgkin lymphoma -- PET/CT -- tuberculosis 1
- 1p21.1p12 -- chromosomal deletion -- congenital diaphragmatic hernia -- etiology -- genetics -- hydrops fetalis -- interrupted aortic arch 1
- 22q duplication -- esophageal atresia -- VACTERL 1
- 3D ultrasound -- autosomal recessive Robinow syndrome -- genital hypoplasia -- hypertelorism -- prenatal diagnose -- wide nose 1
- 3D uterine scar scan -- uterine dehiscence -- uterine scan -- uterine scar 1