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Indirect co-culture with tendons or tenocytes can program amniotic epithelial cells towards stepwise tenogenic differentiation

PloS one, 2012-02, Vol.7 (2), p.e30974-e30974

2012

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Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis

PloS one, 2017-12, Vol.12 (12), p.e0189235-e0189235

2017

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Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview

Diagnostics (Basel), 2021-11, Vol.11 (12), p.2239

2021

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Non-invasive prenatal screening: A 20-year experience in Italy

European journal of obstetrics & gynecology and reproductive biology: X, 2019-07, Vol.3, p.100050-100050, Article 100050

2019

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First case of two supernumerary markers derived from chromosome 5 and chromosome 8

Molecular cytogenetics, 2022-06, Vol.15 (1), p.1-26, Article 26

2022

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Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report

Journal of medical case reports, 2021-04, Vol.15 (1), p.208-208, Article 208

2021

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Human Second Trimester Amniotic Fluid Cells are Able to Create Embryoid Body-Like Structures in Vitro and to Show Typical Expression Profiles of Embryonic and Primordial Germ Cells

Cell transplantation, 2014-01, Vol.23 (12), p.1501-1515

2014

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Prolonged in vitro expansion partially affects phenotypic features and osteogenic potential of ovine amniotic fluid-derived mesenchymal stromal cells

Cytotherapy (Oxford, England), 2013-08, Vol.15 (8), p.930-950

2013

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Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence?

Cytogenetic and genome research, 2019-01, Vol.158 (3), p.121-125

2019

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Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures

Cytogenetic and genome research, 2015-01, Vol.146 (2), p.115-119

2015

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Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment

Pediatrics (Evanston), 2012-01, Vol.129 (1), p.e183-e188

2012

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An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations

Molecular syndromology, 2017-01, Vol.8 (1), p.42-44

2017

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Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation

Gene, 2012-08, Vol.504 (1), p.107-110

2012

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Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3

Journal of genetics, 2018-03, Vol.97 (1), p.311-317

2018

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Optimal cut-offs for down syndrome contingent screening in a population of 10156 pregnant women

Prenatal diagnosis, 2012-12, Vol.32 (12), p.1147

2012

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16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer

Gene, 2012-05, Vol.498 (2), p.328-331

2012

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Aneuploidy screening using circulating fetal cells in maternal blood by dual‐probe FISH protocol: a prospective feasibility study on a series of 172 pregnant women

Molecular genetics & genomic medicine, 2016-11, Vol.4 (6), p.634-640

2016

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Optimal cut-offs for down syndrome contingent screening in a population of 10 156 pregnant women

Prenatal diagnosis, 2012-12, Vol.32 (12), p.1147-1150

2012

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16p13.3 microduplication syndrome: A new characteristic case without intellectual disability

Gene reports, 2016-09, Vol.4, p.218-221

2016

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Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate

Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1056-n/a

2020

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De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects

Clinical dysmorphology, 2013-07, Vol.22 (3), p.132-134

2013

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Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson

Clinical dysmorphology, 2012-07, Vol.21 (3), p.137-140

2012

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Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus

European journal of medical genetics, 2011-05, Vol.54 (3), p.333-336

2011

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A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh

Journal of genetic syndrome & gene therapy, 2013, Vol.4 (11)

Militti, Lucia

2013

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Discovering a familial Xp11.4 microduplication: Does the mother matter?

Meta Gene, 2018-06, Vol.16, p.90-95

2018

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Indirect co-culture with tendons or tenocytes can program amniotic epithelial cells towards stepwise tenogenic differentiation

Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis

Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview

Non-invasive prenatal screening: A 20-year experience in Italy

First case of two supernumerary markers derived from chromosome 5 and chromosome 8

Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report

Human Second Trimester Amniotic Fluid Cells are Able to Create Embryoid Body-Like Structures in Vitro and to Show Typical Expression Profiles of Embryonic and Primordial Germ Cells

Prolonged in vitro expansion partially affects phenotypic features and osteogenic potential of ovine amniotic fluid-derived mesenchymal stromal cells

Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence?

Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures

Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment

An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations

Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation

Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3

Optimal cut-offs for down syndrome contingent screening in a population of 10156 pregnant women

16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer

Aneuploidy screening using circulating fetal cells in maternal blood by dual‐probe FISH protocol: a prospective feasibility study on a series of 172 pregnant women

Optimal cut-offs for down syndrome contingent screening in a population of 10 156 pregnant women

16p13.3 microduplication syndrome: A new characteristic case without intellectual disability

Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate

De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects

Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson

Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus

A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh

Discovering a familial Xp11.4 microduplication: Does the mother matter?

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