Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3–7p15.3, including TWIST1 gene – a case report
Keyword(s):
De Novo
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2011 ◽
Vol 96
(5)
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pp. 1160-1164
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2014 ◽
Vol 210
(12)
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pp. 1090-1094
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2016 ◽
Vol 26
(2)
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pp. 125-128