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
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author: Anna Kucińska-Chahwan Grzegorz Jakiel Diana Massalska Julia Bijok Aleksander Jamsheer |
| Publication date | July 1, 2014 |
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