Familial absence of the trapezius muscle with associated shoulder girdle abnormalities

Preserved visual imagery and categorization in a case of associative visual agnosia.

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Methylphenidate, interstimulus interval, and reaction time performance of children with attention deficit/hyperactivity disorder: a pilot study.

Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence·2009

Developmental dyscalculia is a familial learning disability.

Journal of learning disabilities·2004

Arithmetic skills in kindergarten children with developmental language disorders.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2001

Developmental dyscalculia.

Pediatric neurology·2001

Cognition, attention, and behavior in Prader-Willi syndrome.

Journal of child neurology·2001

Two Truncating MITF Variants Expand the Phenotypic Spectrum of COMMAD Syndrome.

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Compound-Heterozygous PLVAP Missense Variants Associated With Attenuated Protein-Losing Enteropathy (DIAR10).

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A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

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A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.

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A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

Clinical genetics·2026

Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

Clinical genetics·2026

Clinic-Based Proportion of Psoriatic Arthritis and HLA-B27 Distribution in Korean Psoriasis Patients: A Retrospective Study.

Annals of dermatology·2026

Amyloid-β plaque diversity across brain regions in Alzheimer's disease and its relation to major clinicopathological traits.

Acta neuropathologica·2026

Asthma: From Phenotypes to Endotypes-Beyond Type 2 Inflammation.

Respirology (Carlton, Vic.)·2026

Sample size effects on allele diversity, rare-allele recovery, and forensic parameters of 22 autosomal STRs in a cohort of 8,237 Argentines.

International journal of legal medicine·2026

Low-BMI sarcopenic obesity in adults with profound intellectual and multiple disabilities: A body composition analysis using bioelectrical impedance analysis and CT.

Brain & development·2026

Clinical characteristics and genetic analysis of children with corpus callosum abnormalities.

Pediatrics and neonatology·2026

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Familial absence of the trapezius muscle with associated shoulder girdle abnormalities

Related Concept Videos

Preserved visual imagery and categorization in a case of associative visual agnosia.

Methylphenidate, interstimulus interval, and reaction time performance of children with attention deficit/hyperactivity disorder: a pilot study.

Developmental dyscalculia is a familial learning disability.

Arithmetic skills in kindergarten children with developmental language disorders.

Developmental dyscalculia.

Cognition, attention, and behavior in Prader-Willi syndrome.

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Related Experiment Videos

Familial absence of the trapezius muscle with associated shoulder girdle abnormalities

Abstract:

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