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Prenatal Diagnosis of 8p23 Deletion Syndrome by Single Nucleotide Polymorphism Microarray

Crossref DOI link: https://doi.org/10.1007/s40556-021-00322-6

Published Online: 2023-05-05

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Kaymak, Didem https://orcid.org/0000-0002-2755-1932
Alpay, Verda https://orcid.org/0000-0002-5937-0220
Başıbüyük, Zafer

Davutoğlu, Ebru Alıcı https://orcid.org/0000-0003-1634-0117
Madazlı, Riza https://orcid.org/0000-0002-6400-1964
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Version of Record valid from 2023-05-05

Text and Data Mining valid from 2021-12-01

Version of Record valid from 2021-12-01
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Article History

Received: 2 June 2021

Accepted: 27 September 2021

First Online: 22 October 2021

Declarations

:

: The authors declare that they have no conflicts of interest.

: Consent from the patient has been taken to publish the respective case details and photographs.