Marco Baccarin

Marco Baccarin

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Marco Baccarin

Marco Baccarin

Publications by authors named "Marco Baccarin"

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Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review.

Clin Genet 2019 Mar 14. Epub 2019 Mar 14.

Interdepartmental Program "Autism 0-90", "Gaetano Martino" University Hospital, University of Messina, Messina, Italy.

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http://dx.doi.org/10.1111/cge.13537DOI Listing
March 2019

Prenatal upper-limb mesomelia and 2q31.1 microdeletions affecting the regulatory genome.

Genet Med 2018 11;20(11):1483-1484

Medical Genetics Unit, Fondazione, Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.

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http://dx.doi.org/10.1038/gim.2018.19DOI Listing
November 2018

Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1.

Cytogenet Genome Res 2017 20;153(2):73-80. Epub 2017 Dec 20.

Laboratory of Medical Genetics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

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http://dx.doi.org/10.1159/000485226DOI Listing
February 2018

Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.

BMC Med Genet 2017 10 18;18(1):115. Epub 2017 Oct 18.

Division of Pathology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Department of Pathophysiology & Transplantation, Università degli Studi di Milano, Milan, Italy.

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http://dx.doi.org/10.1186/s12881-017-0470-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5648441PMC
October 2017

7p22.1 microduplication syndrome: Refinement of the critical region.

Eur J Med Genet 2017 Feb 16;60(2):114-117. Epub 2016 Nov 16.

Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S17697212163015
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http://dx.doi.org/10.1016/j.ejmg.2016.11.005DOI Listing
February 2017

Prenatal diagnosis of Simpson-Golabi-Behmel syndrome.

Am J Med Genet A 2016 12 9;170(12):3258-3264. Epub 2016 Sep 9.

Clinical Genetics Unit, Fondazione IRCCS Cà Granda, Ospedale Maggiore Policlinico, Milano, Italy.

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http://dx.doi.org/10.1002/ajmg.a.37873DOI Listing
December 2016

Insights into 6q21-q22: Refinement of the critical region for acro-cardio-facial syndrome.

Congenit Anom (Kyoto) 2016 Jul;56(4):187-189

Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy.

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http://dx.doi.org/10.1111/cga.12164DOI Listing
July 2016

Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene.

Am J Med Genet A 2016 May 11;170A(5):1257-61. Epub 2016 Jan 11.

Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

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http://dx.doi.org/10.1002/ajmg.a.37553DOI Listing
May 2016

Impaired Angiogenic Potential of Human Placental Mesenchymal Stromal Cells in Intrauterine Growth Restriction.

Stem Cells Transl Med 2016 Apr 8;5(4):451-63. Epub 2016 Mar 8.

"L. Sacco" Department of Biomedical and Clinical Sciences, Center for Fetal Research Giorgio Pardi, Universitá degli Studi di Milano, Milan, Italy Department of Mother and Child, Luigi Sacco Hospital, Milan, Italy

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http://dx.doi.org/10.5966/sctm.2015-0155DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4798734PMC
April 2016

Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features.

Eur J Med Genet 2016 Jan 15;59(1):39-42. Epub 2015 Dec 15.

Medical Genetics Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

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http://dx.doi.org/10.1016/j.ejmg.2015.12.005DOI Listing
January 2016

Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.

Am J Med Genet A 2015 Jul 6;167(7):1551-9. Epub 2015 Apr 6.

Medical Genetics Unit, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.

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http://dx.doi.org/10.1002/ajmg.a.37063DOI Listing
July 2015

HOXA genes cluster: clinical implications of the smallest deletion.

Ital J Pediatr 2015 Apr 10;41:31. Epub 2015 Apr 10.

Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Commenda 9, Milan, 20122, Italy.

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http://dx.doi.org/10.1186/s13052-015-0137-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4395968PMC
April 2015

Human chorionic villus mesenchymal stromal cells reveal strong endothelial conversion properties.

Differentiation 2012 Jun 31;83(5):260-70. Epub 2012 Mar 31.

Laboratorio di Biologia Vascolare e Medicina Rigenerativa, Centro Cardiologico Monzino, IRCCS, Milano, Italy.

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http://dx.doi.org/10.1016/j.diff.2012.02.006DOI Listing
June 2012