Mosaic genome-wide maternal isodiploidy: an extreme form of imprinting disorder presenting as prenatal diagnostic challenge
Crossref DOI link:
Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY
Barth, Thomas F.
Funding for this research was provided by:
German national BMBF (Ministry of Education and Science)-funded consortium ´Diseases caused by imprinting defects: clinical spectrum and pathogenetic mechanisms´ (FKZ: 01GM1513)