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You searched for: Author/Creator Unolt, MartaLimit your search
- Unolt, Marta [remove] 14
- Medical genetics -- Periodicals 9
- 616.14205 8
- 16q24.3 deletion -- ANKRD11 gene -- atrioventricular septal defect -- congenital heart defect -- KBG syndrome 1
- 22q11.2 -- DiGeorge -- genomic disorder -- multidisciplinary -- syndrome 1
- 22q11.2 deletion syndrome -- cardiac surgery -- cardiology follow‐up -- cardiovascular abnormalities -- congenital heart diseases -- CRKL -- miRNA -- prenatal counseling -- single nucleotide polymorphisms -- TBX1 1
- 22q11.2 deletion syndrome -- chromosome 22q11.2 deletion -- congenital diaphragmatic hernia -- DiGeorge syndrome -- velocardiofacial syndrome -- conotruncal anomaly face syndrome -- microdeletion syndromes -- prenatal diagnosis -- 22q11.2DS 1
- 22q11.2 deletion syndrome -- congenital heart disease -- crossed pulmonary arteries -- genetic syndrome -- pulmonary artery abnormalities 1
- 22q11.2 deletion syndrome -- schizophrenia -- myoclonic epilepsy -- parkinson's disease -- left-handedness 1
- 571.3 1
- 616.042 1