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Levels of 5-hydroxytryptophol in cerebrospinal fluid from alcoholics determined by gas chromatography-mass spectrometry.

Biochemical pharmacology·2010

Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome.

Journal of medical genetics·2009

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BMJ case reports·2026

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The journal of prevention of Alzheimer's disease·2026

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Frontiers in oncology·2026

Caenorhabditis elegans H1 histone variant HIL-2 is positively regulated by nutrient availability and insulin/IGF signaling but does not affect development.

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A systematic review investigating the safety and efficacy of intravenous iron in people with ND-CKD who are iron deficient but not anaemic.

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BMJ case reports·2026

Related Experiment Videos

Failure to diagnose carbohydrate-deficient glycoprotein syndrome prenatally

Related Concept Videos

Clinical segmentation in 22q11.2 deletion syndrome: Cognitive impairments and additional genetic load.

Clinical presentations of 23 half-siblings from a mosaic neurofibromatosis type 1 sperm donor.

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Failure to diagnose carbohydrate-deficient glycoprotein syndrome prenatally

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