Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time

Por Sinem Yalçıntepe, Hakan Gürkan, Engin Atlı, Niyazi Cenk Sayın, Ümit Nusret Başaran
Publicado em 2020-09-01

Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies

Por Emine Ikbal Atli, Engin Atli, Cihan Inan, Gülizar Fusun Varol, Cisem Mail, Esra Altan Erbilen, Sinem Yalcintepe, Selma Demir, Hakan Gurkan
Publicado em 2022-05-01