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2013 | 1 |
2014 | 1 |
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Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite.
BMC Med Genet. 2014 Dec 4;15:128. doi: 10.1186/s12881-014-0128-z.
BMC Med Genet. 2014.
PMID: 25472632
Free PMC article.
Novel FOXF1 deep intronic deletion causes lethal lung developmental disorder, alveolar capillary dysplasia with misalignment of pulmonary veins.
Szafranski P, Yang Y, Nelson MU, Bizzarro MJ, Morotti RA, Langston C, Stankiewicz P.
Szafranski P, et al.
Hum Mutat. 2013 Nov;34(11):1467-71. doi: 10.1002/humu.22395. Epub 2013 Sep 4.
Hum Mutat. 2013.
PMID: 23943206
Free PMC article.
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