Publications by authors named "Maria A Lacruz-Rengel"

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Clinical and Genetic Aspects of Phelan-McDermid Syndrome: An Interdisciplinary Approach to Management.
Francisco Cammarata-Scalisi, Michele Callea, Diego Martinelli, Colin Eric Willoughby, Antonio Cárdenas Tadich, María Angelina Lacruz-Rengel

Genes (Basel)· March 2022

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[Wolf-Hirschhorn syndrome. Description of five cases characterized by means of single nucleotide polymorphism microarrays].
Francisco Cammarata-Scalisi, Raquel Blanco Lago, Pilar Barruz Galián, Pablo Lapunzina Badía, Dianora Araque, María A Lacruz-Rengel

Arch Argent Pediatr· August 2019

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[Isotretinoin embryopathy: An entity that can be avoided].
Francisco Cammarata-Scalisi, Dairelis Nieves, Andrea Avendaño, María A Lacruz-Rengel, Karelys Alviárez

Arch Argent Pediatr· April 2018

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[Clinical and molecular study in a family with cleidocranial dysplasia].
Michele Callea, Fabiana Fattori, Enrico S Bertini, Izzet Yavuz, Emanuele Bellacchio, María A Lacruz-Rengel

Arch Argent Pediatr· December 2017

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[Mosaic trisomy 18. Series of cases].
Francisco Cammarata-Scalisi, María A Lacruz-Rengel, Dianora Araque, Gloria Da Silva, Andrea Avendaño

Arch Argent Pediatr· June 2017

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[Metatropic dysplasia in a girl with c.1811_1812delinsAT mutation in exon 11 of the TRPV4 gene not previously reported].
Francisco Cammarata-Scalisi, Uta Matysiak-Scholze, Jessica Heinze, Albaro Barrera, María Angelina Lacruz-Rengel

Arch Argent Pediatr· January 2015

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[Clinical and molecular study of the Noonan syndrome].
Francisco Cammarata-Scalisi, Giovanni Neri, Maria Grazia Pomponi, Giorgia Mancano, Gloria Da Silva, María Angelina Lacruz-Rengel

Invest Clin· December 2012

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