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Genes|October 27, 2022
Phenotypic Spectrum and Molecular Findings in 17 ATR-X Syndrome Italian Patients: Some New InsightsAlessandro Vaisfeld, Sara Taormina, Alessandro Simonati, et al.
The Journal of Clinical Investigation|December 4, 2012
Fragile X syndrome: causes, diagnosis, mechanisms, and therapeuticsClaudia Bagni, Flora Tassone, Giovanni Neri, et al.
Pediatric Pathology & Molecular Medicine|April 11, 2002
Cholesterol and development: the RSH ("Smith-Lemli-Opitz") syndrome and related conditionsJohn M Opitz, Enid Gilbert-Barness, Jeanie Ackerman, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
ADAM "sequence" part II: hypothesis and speculationJohn M Opitz, Dennis R Johnson, Enid F Gilbert-Barness
American Journal of Medical Genetics. Part A|June 18, 2016
Recognizable facial features in patients with alternating hemiplegia of childhoodFiorella Gurrieri, Francesco Danilo Tiziano, Giuseppe Zampino, et al.
American Journal of Medical Genetics|December 28, 2002
Limb anomalies: Developmental and evolutionary aspectsFiorella Gurrieri, Klaus W Kjaer, Eugenio Sangiorgi, et al.
Sensors (Basel, Switzerland)|October 24, 2018
Photo-Electrochemical Sensing of Dopamine by a Novel Porous TiO₂ Array-Modified Screen-Printed Ti ElectrodeFrancesco Tavella, Claudio Ampelli, Salvatore Gianluca Leonardi, et al.
European Journal of Human Genetics : EJHG|January 17, 2008
XLMR genes: update 2007Pietro Chiurazzi, Charles E Schwartz, Jozef Gecz, et al.
Cancer Biomarkers : Section a of Disease Markers|December 29, 2006
The use of microsatellite instability, immunohistochemistry and other variables in determining the clinical significance of MLH1 and MSH2 unclassified variants in Lynch syndromeEmanuela Lucci-Cordisco, Luigi Boccuto, Giovanni Neri, et al.
Nanomaterials (Basel, Switzerland)|November 24, 2017
Iron-Based Nanomaterials/Graphene Composites for Advanced Electrochemical SensorsKaveh Movlaee, Mohmmad Reza Ganjali, Parviz Norouzi, et al.
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