Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesis

Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results

(2014) Francesca R. Grati et al.   GENETICS IN MEDICINE

De novosmall supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches

(2014) Francesca Malvestiti et al.   PRENATAL DIAGNOSIS

Cytogenetic follow-up of chromosomal mosaicism detected in first-trimester prenatal diagnosis

(2014) Paola Battaglia et al.   PRENATAL DIAGNOSIS

Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis

(2014) Francesca Grati   Journal of Clinical Medicine

Integration of Noninvasive DNA Testing for Aneuploidy into Prenatal Care: What Has Happened Since the Rubber Met the Road?

(2013) D. W. Bianchi et al.   CLINICAL CHEMISTRY

Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype

(2012) Jun Liao et al.   PRENATAL DIAGNOSIS

Application of a new molecular technique for the genetic evaluation of products of conception

(2012) Francesca R. Grati et al.   PRENATAL DIAGNOSIS

Diagnostic Implications of Excessive Homozygosity Detected by SNP-Based Microarrays: Consanguinity, Uniparental Disomy, and Recessive Single-Gene Mutations

(2011) Hutton M. Kearney et al.   CLINICS IN LABORATORY MEDICINE

CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy

(2010) AJ Dawson et al.   CLINICAL GENETICS

Rare finding of 2n/4n mixoploidy in mother and fetus with severe immune hydrops

(2009) A. Sharma et al.   CYTOGENETIC AND GENOME RESEARCH