Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00412-022-00782-3.pdf
Reference65 articles.
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3. Balkan M, Akbas H, Isi H, Oral D, Turkyılmaz A, Kalkanli S, Simsek S, Fidanboy M, Alp MN, Gedik A, Budak T (2010) Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey. Genet Mol Res 9:1094–1103. https://doi.org/10.4238/vol9-2gmr827
4. Bassett AS (1992) Chromosomal aberrations and schizophrenia. Br J Psychiatry 161:323–334
5. Bohîlţea RE, Cîrstoiu MM, Nedelea FM, Turcan N, Georgescu TA, Munteanu O, Baroş A, Anca Maria Istrate-Ofiţeru AMI, Berceanu C (2020) Case report of a novel phenotype in 18q deletion syndrome. Rom J Morphol Embryol 61:905–910. https://doi.org/10.47162/RJME.61.3.29
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