Muscular dystrophy: genetic counselling and family planning

Re-evaluation of the dysequilibrium syndrome.

Acta neurologica Scandinavica·2010

Prevalence and associated impairments of mild mental retardation in six- to ten-year old children in Pakistan: a prospective study.

Acta paediatrica (Oslo, Norway : 1992)·2002

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Acta dermato-venereologica·1999

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.

Annals of neurology·1999

Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding.

Clinical genetics·1998

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene.

Human mutation·1998

Short- and long-term effects of a 12-week intensive functional restoration programme in individuals work-disabled by chronic spinal pain.

Scandinavian journal of rehabilitation medicine. Supplement·2000

The contribution of molecular genetics in the diagnosis and management of neuromuscular disorders.

Scandinavian journal of rehabilitation medicine. Supplement·1999

Daily activities in women with rheumatoid arthritis. Aspects of patient education, assistive devices and methods for disability and impairment assessment.

Scandinavian journal of rehabilitation medicine. Supplement·1997

Prevention of occupational musculo-skeletal injuries. Labour Inspectorate investigation.

Scandinavian journal of rehabilitation medicine. Supplement·1996

Longitudinal studies of dependence in daily life activities among elderly persons.

Scandinavian journal of rehabilitation medicine. Supplement·1996

An overview of psychosocial and behavioral factors in neck-and-shoulder pain.

Scandinavian journal of rehabilitation medicine. Supplement·1995

Obesity and reduced renal corticomedullary differentiation on T1 mapping: a population-based UK Biobank study.

International urology and nephrology·2026

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Biology of sex differences·2026

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Ophthalmology science·2026

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Journal of assisted reproduction and genetics·2026

Related Experiment Videos

Muscular dystrophy: genetic counselling and family planning

Related Concept Videos

Re-evaluation of the dysequilibrium syndrome.

Prevalence and associated impairments of mild mental retardation in six- to ten-year old children in Pakistan: a prospective study.

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.

Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding.

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene.

Short- and long-term effects of a 12-week intensive functional restoration programme in individuals work-disabled by chronic spinal pain.

The contribution of molecular genetics in the diagnosis and management of neuromuscular disorders.

Daily activities in women with rheumatoid arthritis. Aspects of patient education, assistive devices and methods for disability and impairment assessment.

Prevention of occupational musculo-skeletal injuries. Labour Inspectorate investigation.

Longitudinal studies of dependence in daily life activities among elderly persons.

An overview of psychosocial and behavioral factors in neck-and-shoulder pain.

Obesity and reduced renal corticomedullary differentiation on T1 mapping: a population-based UK Biobank study.

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

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Muscular dystrophy: genetic counselling and family planning

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