A rare <i>de novo</i> contiguous 15q11.1-q13.3 duplication with tetrasomy (CN=4) and adjacent trisomy (CN=3) associated with severe global developmental delay, autism spectrum disorder, and subclinical epileptiform discharges: a case report and literature review. [PDF]
Zhou X +6 more
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Fetal Biometric Parameters in USG for Early Detection of Fetal Growth Restriction. [PDF]
Rai H +5 more
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Effectiveness of AI-enhanced colonoscopy: A case-control study using real world evidence in a young screening age population. [PDF]
Alahmad MA +10 more
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A rare case of cauda equina paraganglioma histologically simulating ependymoma. [PDF]
Alyousef EMK +5 more
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Results of Chromosomal Microarray Need to Always Be Checked by (Molecular) Cytogenetics-Even If They Seem to Be Simple Deletions. [PDF]
Liehr T +7 more
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Clinical and molecular cytogenetic findings of cat eye syndrome and a 2-year-old patient with congenital aural atresia and hearing loss. [PDF]
Xu L +6 more
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Dandy's vein decompression for trigeminal neuralgia: A rare venous conflict causing intractable facial pain. [PDF]
Rahman MM +5 more
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The effects of EXOPULSE Mollii Suit in patients with fibromyalgia: a double-blind randomized sham-controlled trial (EXOFIB2). [PDF]
Riachi N +8 more
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Role of immunohistochemistry in differentiating between reactive and malignant lymphoid hyperplasia - A cross-sectional study. [PDF]
Chourasia S, Badkur S, Kumar A, Shah M.
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