Dual independent genetic etiologies in a lethal complex malformation phenotype
Ultraschall Med
.
2020 Apr;41(2):112-114.
doi: 10.1055/a-1104-3625.
Epub 2020 Apr 7.
Authors
Isabel Filges
1
,
Agnes Genewein
2
,
Peter Weber
3
,
Stephanie Meier
1
,
Nikolaus Deigendesch
4
,
Elisabeth Bruder
4
,
Friederike Prüfer
5
,
Sevgi Tercanli
6
Affiliations
1
Medical Genetics, Institute for Medical Genetics and Pathology, University Hospital Basel and University of Basel, Switzerland.
2
Neonatology, University Children's Hospital Basel and University of Basel, Switzerland.
3
Pediatric Neurology and Developmental Medicine, University Children's Hospital Basel and University of Basel, Switzerland.
4
Pathology, Institute for Medical Genetics and Pathology, University Hospital Basel and University of Basel, Switzerland.
5
Pediatric Radiology, University Children's Hospital Basel and University of Basel, Switzerland.
6
Center for Prenatal Ultrasound, Freie Strasse, Basel and University of Basel, Switzerland.
PMID:
32259861
DOI:
10.1055/a-1104-3625
No abstract available
MeSH terms
Abnormalities, Multiple* / genetics
Genotype
Humans
Phenotype*