L. Camurri

发表

Neonatal newborn hearing screening: four years' experience at Ferrara University Hospital (CHEAP project): part 1.

J. Petruccelli, A. Martini, S. Hatzopoulos, 2007, Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale.

Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells

B. Dallapiccola, G. Novelli, F. Sangiuolo, 1996, Human Genetics.

Early second trimester (13 to 20 weeks) transabdominal chorionic villus sampling (TA‐CVS): a safe and alternative method for both high and low risk populations

B. Brambati, L. Tului, L. Camurri, 2002, Prenatal diagnosis.

First-trimester fetal reduction to a singleton infant or twins: outcome in relation to the final number and karyotyping before reduction by transabdominal chorionic villus sampling.

B. Brambati, L. Tului, L. Camurri, 2004, American journal of obstetrics and gynecology.

Sister chromatid exchanges in workers exposed to low doses of styrene.

L. Camurri, S. Candela, S. Codeluppi, 1984, Basic life sciences.

Chromosomal aberrations and sister-chromatid exchanges in workers exposed to styrene.

L. Camurri, C. Pedroni, S. Codeluppi, 1983, Mutation research.

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011

L. Bernardini, A. Novelli, O. Zuffardi, 2012, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The contingent use of cell-free fetal DNA for prenatal screening of trisomies 21, 18, 13 in pregnant women within a national health service: A budget impact analysis

F. Prefumo, L. Camurri, D. Paolini, 2019, PloS one.

Are chromosome aberrations in circulating lymphocytes predictive of future cancer onset in humans? Preliminary results of an Italian cohort study.

S. Bonassi, C. Lando, R. Puntoni, 1995, Cancer genetics and cytogenetics.

A three‐year follow‐up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally

L. Camurri, A. Chiesi, Annalisa Chiesi, 1991, Prenatal diagnosis.

D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p)

R. Tenconi, G. Floridia, M. Clementi, 1993, Human Genetics.

Influence of sex on cytogenetic end points: evidence from a large human sample and review of the literature.

S. Bonassi, C. Lando, R. Barale, 1995, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Chromosome Analysis of First Trimester Chorionic Villi Sampled by Chorionscope

L. Camurri, G. Ghirardini, G. Terzoli, 1985 .

Exocoelomic space, limb reduction, and CVS

L. Camurri, G. Ghirardini, 1991, The Lancet.

Chorionic Villi Sampling by Means of a New Endoscopic Device

L. Camurri, P. Agnelli, C. Gualerzi, 1985 .

A familial case of chromosome 16p variant.

L. Camurri, F. Franchi, G. Croci, 1991, Journal of medical genetics.

Yq deletions and AZF locus: molecular analysis in two fetuses with non familial homogeneous Yq rearrangements.

G. Novelli, L. Camurri, M. Gennarelli, 1993, Genetic counseling.

Chromosomal microarray as first‐tier approach in low‐risk pregnancies: detection rate should not be the only criterion for its application

L. Sinibaldi, L. Camurri, M. Gentile, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.