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Publikováno v:
Genetic counseling (Geneva, Switzerland). 26(2)
We present a 9 month-old baby girl with de novo pure interstitial duplication 1q. The girl has dysmorphic craniofacial features as well as neuromotor retardation, multiple subcutaneous solid tissue lesions, urogenital anomalies, cardiac defect, liver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1598d1699207a1d9677201998abb31a
https://pubmed.ncbi.nlm.nih.gov/26349187
https://pubmed.ncbi.nlm.nih.gov/26349187
