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American Journal of Medical Genetics. Part A|July 9, 2011
The FRAXopathies: definition, overview, and updateFilomena Pirozzi, Elisabetta Tabolacci, Giovanni Neri
Critical Reviews in Clinical Laboratory Sciences|July 24, 2004
X-linked mental retardation (XLMR): from clinical conditions to cloned genesPietro Chiurazzi, Elisabetta Tabolacci, Giovanni Neri
Fetal and Pediatric Pathology|June 24, 2008
Restrictive dermopathy: report and reviewPawini Khanna, John M Opitz, Enid Gilbert-Barness
Advances in Pediatrics|December 4, 2008
The FG syndromes (Online Mendelian Inheritance in Man 305450): perspective in 2008John M Opitz, James F Smith, Lucia Santoro
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 11, 2011
Lethal osteogenesis imperfecta-like condition with cutis laxa and arterial tortuosity in MZ twins due to a homozygous fibulin-4 mutationLance K Erickson, John M Opitz, Holly Zhou
Sensors (Basel, Switzerland)|January 10, 2019
NO₂ Selective Sensor Based on α-Fe₂O₃ Nanoparticles Synthesized via Hydrothermal TechniqueMokhtar Hjiri, Mohamed Salah Aida, Giovanni Neri
Current Opinion in Pediatrics|November 25, 2003
Understanding the biological underpinnings of fragile X syndromePietro Chiurazzi, Giovanni Neri, Ben A Oostra
International Journal of Molecular Sciences|February 23, 2011
Biomarkers in rare disorders: the experience with spinal muscular atrophyFrancesco D Tiziano, Giovanni Neri, Christina Brahe
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 21, 2022
Dermatological manifestations, management, and care in RASopathiesMaria Ines Kavamura, Chiara Leoni, Giovanni Neri
American Journal of Medical Genetics. Part A|September 25, 2004
A case of Kabuki (Niikawa-Kuroki) syndrome associated with manifestations resembling C-trigonocephaly syndromeGrace David, David Sillence, Robert Hardwick, et al.
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