[Inherited mental retardation in the male caused by a structural X chromosomal defect]

Obesity in 4-year-old children more prevalent in girls and in municipalities with a low socioeconomic level.

Acta paediatrica (Oslo, Norway : 1992)·2006

Solar disinfection of water for diarrhoeal prevention in southern India.

Archives of disease in childhood·2006

Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.

Journal of medical genetics·2005

Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twins.

Journal of internal medicine·2004

Hereditary transthyretin amyloidosis from a Scandinavian perspective.

Journal of internal medicine·2003

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.

Neurology·2002

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

Lakartidningen·2026

[Rare manifestations of giant cell arteritis].

Lakartidningen·2026

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

Lakartidningen·2026

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

Lakartidningen·2026

[Postoperative atrial fibrillation after open heart surgery].

Lakartidningen·2026

[Interaction between psychotic patients and AI-driven chatbots].

Lakartidningen·2026

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Molecular biology and evolution·2026

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Brain communications·2026

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Brain, behavior, and immunity·2026

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

Legal medicine (Tokyo, Japan)·2026

LINE-1 repeats are a defining feature of the Xce.

Proceedings of the National Academy of Sciences of the United States of America·2026

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

JCI insight·2026

Related Experiment Videos

[Inherited mental retardation in the male caused by a structural X chromosomal defect]

Related Concept Videos

Obesity in 4-year-old children more prevalent in girls and in municipalities with a low socioeconomic level.

Solar disinfection of water for diarrhoeal prevention in southern India.

Impact of homozygosity for an amyloidogenic transthyretin mutation on phenotype and long term outcome.

Discordant penetrance of the trait for familial amyloidotic polyneuropathy in two pairs of monozygotic twins.

Hereditary transthyretin amyloidosis from a Scandinavian perspective.

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.

[Upper tract urothelial carcinoma - regional differences observed in several quality indicators].

[Rare manifestations of giant cell arteritis].

[Neoehrlichiosis in rituximab-treated patients with MS in Sweden].

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

[Postoperative atrial fibrillation after open heart surgery].

[Interaction between psychotic patients and AI-driven chatbots].

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

LINE-1 repeats are a defining feature of the Xce.

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

Related Experiment Videos

[Inherited mental retardation in the male caused by a structural X chromosomal defect]

Related Concept Videos

Related Articles