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Does cystic fibrosis neonatal screening detect atypical CF forms? Extended genetic characterization and 4-year clinical follow-up.
Clin Genet. 2007 Jul;72(1):39-46. doi: 10.1111/j.1399-0004.2007.00825.x.
Clin Genet. 2007.
PMID: 17594398
Comparison of two different protocols of neonatal screening for cystic fibrosis.
Narzi L, Lucarelli M, Lelli A, Grandoni F, Lo Cicero S, Ferraro A, Matarazzo P, Delaroche I, Quattrucci S, Strom R, Antonelli M.
Narzi L, et al. Among authors: delaroche i.
Clin Genet. 2002 Sep;62(3):245-9. doi: 10.1034/j.1399-0004.2002.620311.x.
Clin Genet. 2002.
PMID: 12220442
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Incidence of chromosome abnormalities and clinical significance of karyotype in de novo acute myeloid leukemia.
Stasi R, Del Poeta G, Masi M, Tribalto M, Venditti A, Papa G, Nicoletti B, Vernole P, Tedeschi B, Delaroche I, et al.
Stasi R, et al. Among authors: delaroche i.
Cancer Genet Cytogenet. 1993 May;67(1):28-34. doi: 10.1016/0165-4608(93)90040-s.
Cancer Genet Cytogenet. 1993.
PMID: 8504396
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Fetal translocation between chromosomes 2, 18, and 21 resolved by fish.
Delaroche I, Sabani M, Calabrese G, Mingarelli R, Palka G, Dallapiccola B.
Delaroche I, et al.
Prenat Diagn. 1995 Mar;15(3):278-81. doi: 10.1002/pd.1970150312.
Prenat Diagn. 1995.
PMID: 7784387
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Regional mapping of hexokinase-1 within the short arm of chromosome 10.
Dallapiccola B, Novelli G, Micara G, Delaroche I, Moric-Petrovic S, Magnani M.
Dallapiccola B, et al. Among authors: delaroche i.
Hum Hered. 1984;34(3):156-60. doi: 10.1159/000153453.
Hum Hered. 1984.
PMID: 6590458
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Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
Delaroche I, Bruni L, Giannotti A, Giampaolo R, Aebischer ML.
Delaroche I, et al.
Helv Paediatr Acta. 1984 May;39(2):161-6.
Helv Paediatr Acta. 1984.
PMID: 6543839
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[Monosomy 18p syndrome with holoprosencephaly].
Carratù A, Delaroche I, Tomassini P, Bruni L.
Carratù A, et al. Among authors: delaroche i.
Minerva Pediatr. 1983 Dec 31;35(23-24):1225-8.
Minerva Pediatr. 1983.
PMID: 6674744
Italian.
No abstract available.
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Phenotypic and genotypic characteristics of new euploid-diploid lymphoblastoid B cell lines EBV+, normal human bone marrow derived, spontaneously overgrown in vitro.
Bertolini L, Aebischer ML, Ameglio F, Angeloni A, Delaroche I, Faggioni A, Fruscalzo A, Gorini G, Serafino A, Starace G, Tabilio A.
Bertolini L, et al. Among authors: delaroche i.
J Virol Methods. 2005 Jun;126(1-2):91-100. doi: 10.1016/j.jviromet.2005.01.029.
J Virol Methods. 2005.
PMID: 15847924
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