Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sander Pajusalu"'
Autor:
Karin Asser, Sander Pajusalu, Pille Tammur, Konstantin Ridnõi, Ustina Šamarina, Kai Muru, Ferenc Szirko, Tiia Reimand, Eva-Liina Ustav, Katrin Õunap, Maria Keernik, Tiina Kahre, Triin Mölter-Väär
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Background Introduction of cell‐free fetal DNA (cff‐DNA) testing in maternal blood opened possibilities to improve the performance of combined first‐trimester screening (cFTS) in terms of better detection of trisomies and lowering invasive test
Publikováno v:
Clinical Case Reports
Key Clinical Message 3q26.33‐3q27.2 microdeletion can be classified as a clinical entity characterized by intrauterine growth retardation, feeding problems in infancy, short stature, intellectual disability, hypotonia, dysmorphic facial features (m