دورية أكاديمية
Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype
| العنوان: | Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotype |
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| المؤلفون: | Wang, XuezhenAff1, Aff2, Guo, LiliAff1, Aff2, Zhang, BeiAff1, Aff2, Aff3, Wu, JiebinAff1, Aff2, Aff3, Sun, YuAff3, Aff4, Tao, HuiminAff2, Aff3, Sha, Jing, Zhai, JingfangAff1, Aff2, Aff3, IDs13039022006279_cor8, Liu, MinAff2, Aff3, IDs13039022006279_cor9 |
| المصدر: | Molecular Cytogenetics. 15(1) |
| قاعدة البيانات: | Springer Nature Journals |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 17558166 |
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| DOI: | 10.1186/s13039-022-00627-9 |