Kath D. Smith

Truro, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 17 publications

Recommendations for occupational therapy interventions for adults with ADHD: a consensus statement from the UK adult ADHD network.

Recommendations for occupational therapy interventions for adults with ADHD: a consensus statement from the UK adult ADHD network.

Journal: BMC psychiatry

Published: June 01, 2020

Investigation of fibrillin microfibrils in the canine cruciate ligament in dogs with different predispositions to ligament rupture.

Investigation of fibrillin microfibrils in the canine cruciate ligament in dogs with different predispositions to ligament rupture.

Journal: Research in veterinary science

Published: February 27, 2020

Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1.

Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: December 08, 2018

Novel PLS3 variants in X-linked osteoporosis: Exploring bone material properties.

Novel PLS3 variants in X-linked osteoporosis: Exploring bone material properties.

Journal: American journal of medical genetics. Part A

Published: January 10, 2018

Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability.

Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability.

Journal: American journal of medical genetics. Part A

Published: December 18, 2017

Clinical and molecular characterization of the first familial report of 1p32 microdeletion.

Clinical and molecular characterization of the first familial report of 1p32 microdeletion.

Journal: Clinical dysmorphology

Published: December 15, 2017

Autism and heritable bone fragility: A true association?

Autism and heritable bone fragility: A true association?

Journal: Bone reports

Published: December 04, 2017

Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy.

Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy.

Journal: Clinical dysmorphology

Published: October 19, 2016

Inherited duplication of the short arm of chromosome 18p11.32-p11.31 associated with developmental delay/intellectual disability.

Inherited duplication of the short arm of chromosome 18p11.32-p11.31 associated with developmental delay/intellectual disability.

Journal: Clinical dysmorphology

Published: August 20, 2015

Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability.

Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability.

Journal: Clinical dysmorphology

Published: August 13, 2015

Copy number variants in association with type 1 collagenopathy: Atypical osteogenesis imperfecta.

Copy number variants in association with type 1 collagenopathy: Atypical osteogenesis imperfecta.

Journal: American journal of medical genetics. Part A

Published: June 25, 2015

A novel de novo 20q13.32-q13.33 deletion in a 2-year-old child with poor growth, feeding difficulties and low bone mass.

A novel de novo 20q13.32-q13.33 deletion in a 2-year-old child with poor growth, feeding difficulties and low bone mass.

Journal: Journal of human genetics

Published: January 05, 2015

Showing 1-12 of 17

Last Updated: 09/26/2026