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Page 1
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans.
Am J Med Genet A. 2021 Mar;185(3):836-840. doi: 10.1002/ajmg.a.62066. Epub 2021 Jan 14.
Am J Med Genet A. 2021.
PMID: 33443296
Free PMC article.
A peculiar mutation in the DNA-binding/dimerization domain of NFIX causes Sotos-like overgrowth syndrome: a new case.
Priolo M, Grosso E, Mammì C, Labate C, Naretto VG, Vacalebre C, Caridi P, Laganà C.
Priolo M, et al. Among authors: naretto vg.
Gene. 2012 Dec 10;511(1):103-5. doi: 10.1016/j.gene.2012.08.040. Epub 2012 Sep 13.
Gene. 2012.
PMID: 22982744
Review.
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When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort.
Scott A, Di Giosaffatte N, Pinna V, Daniele P, Corno S, D'Ambrosio V, Andreucci E, Marozza A, Sirchia F, Tortora G, Mangiameli D, Di Marco C, Romagnoli M, Donati I, Zonta A, Grosso E, Naretto VG, Mastromoro G, Versacci P, Pantaleoni F, Radio FC, Mazza T, Damante G, Papi L, Mattina T, Giancotti A, Pizzuti A, Laberge AM, Tartaglia M, Delrue MA, De Luca A.
Scott A, et al. Among authors: naretto vg.
Genet Med. 2021 Jun;23(6):1116-1124. doi: 10.1038/s41436-020-01093-7. Epub 2021 Feb 10.
Genet Med. 2021.
PMID: 33568805
Free article.
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Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH.
Di Gregorio E, Savin E, Biamino E, Belligni EF, Naretto VG, D'Alessandro G, Gai G, Fiocchi F, Calcia A, Mancini C, Giorgio E, Cavalieri S, Talarico F, Pappi P, Gandione M, Grosso M, Asnaghi V, Restagno G, Mandrile G, Botta G, Silengo MC, Grosso E, Ferrero GB, Brusco A.
Di Gregorio E, et al. Among authors: naretto vg.
Mol Cytogenet. 2014 Nov 19;7(1):82. doi: 10.1186/s13039-014-0082-7. eCollection 2014.
Mol Cytogenet. 2014.
PMID: 25435912
Free PMC article.
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Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.
Lalatta F, Quagliarini D, Folliero E, Cavallari U, Gentilin B, Castorina P, Forzano F, Forzano S, Grosso E, Viassolo V, Naretto VG, Gattone S, Ceriani F, Faravelli F, Gargantini L.
Lalatta F, et al. Among authors: naretto vg.
Eur J Pediatr. 2010 Oct;169(10):1255-61. doi: 10.1007/s00431-010-1221-8. Epub 2010 May 15.
Eur J Pediatr. 2010.
PMID: 20473517
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Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism.
Gironi LC, Colombo E, Brusco A, Grosso E, Naretto VG, Guala A, Di Gregorio E, Zonta A, Zottarelli F, Pasini B, Savoia P.
Gironi LC, et al. Among authors: naretto vg.
Medicina (Kaunas). 2019 Jul 7;55(7):345. doi: 10.3390/medicina55070345.
Medicina (Kaunas). 2019.
PMID: 31284637
Free PMC article.
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