Recurrent CNVs in constitutional CMA: a ClinGen-anchored single-center postnatal and prenatal experience.

Satkın NB, Atlı E, Yalcintepe S, Çelik KM, Gürkan H

Open source

DOI: 10.3389/fgene.2026.1960791
Published: 2026
Container: Frontiers in genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fgene.2026.1960791,
  title = {Recurrent CNVs in constitutional CMA: a ClinGen-anchored single-center postnatal and prenatal experience.},
  author = {Satkın NB and Atlı E and Yalcintepe S and Çelik KM and Gürkan H},
  year = {2026},
  journal = {Frontiers in genetics},
  doi = {10.3389/fgene.2026.1960791},
  url = {https://doi.org/10.3389/fgene.2026.1960791}
}

RIS

TY  - JOUR
TI  - Recurrent CNVs in constitutional CMA: a ClinGen-anchored single-center postnatal and prenatal experience.
AU  - Satkın NB
AU  - Atlı E
AU  - Yalcintepe S
AU  - Çelik KM
AU  - Gürkan H
PY  - 2026
JO  - Frontiers in genetics
DO  - 10.3389/fgene.2026.1960791
UR  - https://doi.org/10.3389/fgene.2026.1960791
ER  -

APA

NB, S., E, A., S, Y., KM, Ç., & H, G. (2026). Recurrent CNVs in constitutional CMA: a ClinGen-anchored single-center postnatal and prenatal experience.. Frontiers in genetics. https://doi.org/10.3389/fgene.2026.1960791

Source records

pubmed · retrieved 2026-11-10T11:39:20.835Z
europe-pmc · retrieved 2026-11-10T11:39:20.840Z
doaj · retrieved 2026-11-10T11:39:20.833Z