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PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.
Eur J Hum Genet. 2015 Dec;23(12):1615-26. doi: 10.1038/ejhg.2015.51. Epub 2015 Apr 8.
Eur J Hum Genet. 2015.
PMID: 25853300
Free PMC article.
Craniosynostosis, psychomotor retardation, and facial dysmorphic features in a Spanish patient with a 4q27q28.3 deletion.
Fernández-Jaén A, Fernández-Perrone AL, Fernández-Mayoralas DM, Calleja-Pérez B, Sánchez-Hombre Mdel C, Fernández EC, López-Martín S.
Fernández-Jaén A, et al.
Childs Nerv Syst. 2014 Dec;30(12):2157-61. doi: 10.1007/s00381-014-2474-8. Epub 2014 Jul 1.
Childs Nerv Syst. 2014.
PMID: 24980605
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Triplication of 1q in Fanconi anemia.
Ferro MT, Vazquez-Mazariego Y, Ramiro S, Sanchez-Hombre MC, Villalon C, Garcia-Sagredo JM, Ulibarrena C, Sastre JL, Roman CS.
Ferro MT, et al. Among authors: sanchez hombre mc.
Cancer Genet Cytogenet. 2001 May;127(1):38-41. doi: 10.1016/s0165-4608(00)00415-5.
Cancer Genet Cytogenet. 2001.
PMID: 11408063
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Nonclonal abnormalities in leukemia.
Vázquez-Mazariego Y, Ramiro S, Steegman JL, García-Sagredo JM, Sánchez-Hombre MC, Ferro MT.
Vázquez-Mazariego Y, et al. Among authors: sanchez hombre mc.
Cancer Genet Cytogenet. 2000 Apr 1;118(1):85-6. doi: 10.1016/s0165-4608(99)00181-8.
Cancer Genet Cytogenet. 2000.
PMID: 10766522
No abstract available.
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