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Bioorganic Chemistry|August 23, 2024
THP as a sensor for the electrochemical detection of H2O2Mariacristina Failla, Angelo Ferlazzo, Vincenzo Abbate, et al.Human Genetics|December 3, 2005
The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12Rosetta Lecce, Marina Murdolo, Gianfranco Gelli, et al.Nature Genetics|February 7, 2012
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibilityDewi Astuti, Mark R Morris, Wendy N Cooper, et al.European Journal of Human Genetics : EJHG|January 22, 2004
Expansion to full mutation of a FMR1 intermediate allele over two generationsAlessandra Terracciano, Maria Grazia Pomponi, Grazia Maria Elisabetta Marino, et al.ACS Applied Materials & Interfaces|May 6, 2022
Role of Heterojunctions of Core-Shell Heterostructures in Gas SensingMuhammad Hamid Raza, Roberto Di Chio, Kaveh Movlaee, et al.Clinical Genetics|November 10, 2019
X-linked intellectual disability: Phenotypic expression in carrier femalesCatherine A Ziats, Charles E Schwartz, Jozef Gecz, et al.The Journal of Molecular Diagnostics : JMD|May 14, 2013
Molecular inversion probe array for the genetic evaluation of stillbirth using formalin-fixed, paraffin-embedded tissueLeslie R Rowe, Harshwardhan M Thaker, John M Opitz, et al.American Journal of Medical Genetics. Part A|October 15, 2013
Elements of morphology: general terms for congenital anomaliesRaoul C Hennekam, Leslie G Biesecker, Judith E Allanson, et al.Nanomaterials (Basel, Switzerland)|April 3, 2021
Synthesis of Silver and Gold Nanoparticles from Rumex roseus Plant Extract and Their Application in Electrochemical SensorsMeryam Chelly, Sabrine Chelly, Rayhane Zribi, et al.American Journal of Medical Genetics. Part A|November 15, 2017
"Minimal" holoprosencephaly in a 14q deletion syndrome patientElvio Della Giustina, Alessandro Iodice, Carlotta Spagnoli, et al.Pageof 33