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Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1–3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry
Published 2016-01-01“…Objectives Facioscapulohumeral muscular dystrophy type 1 (FSHD1) has been genetically linked to reduced numbers (≤8) of D4Z4 repeats at 4q35. Particularly severe FSHD cases, characterised by an infantile onset and presence of additional extra-muscular features, have been associated with the shortest D4Z4 reduced alleles with 1–3 repeats (1–3 DRA). …”
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PCA and PSO based optimized support vector machine for efficient intrusion detection in internet of things
Published 2025-02-01Get full text
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A Resource-Efficient Multi-Entropy Fusion Method and Its Application for EEG-Based Emotion Recognition
Published 2025-01-01Get full text
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مدى وعى أعضاء هیئة التدریس بجامعة المنوفیة بالانتحال العلمى : دراسة استکشافیة
Published 2020-01-01Get full text
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An Enigmatic Wild Passerine Mortality Event in the Eastern United States
Published 2025-01-01Get full text
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