Merel Klaassens
Maastricht, LI, Netherlands
Last Updated: 09/26/2026
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Found 10 publications
Weight and Infantile Blount Disease: Insights from a Rural Ghanaian Cohort.
Journal: JB & JS open access
Published: January 12, 2026
Neuropathic Pain and Enlarged Nerves in Adult Noonan Syndrome and Noonan Syndrome With Multiple Lentigines: Health-Related Quality of Life and Neurologic Symptoms.
Journal: American journal of medical genetics. Part A
Published: August 12, 2025
The importance of early recognition of Prader-Willi syndrome
Journal: Nederlands tijdschrift voor geneeskunde
Published: May 15, 2024
Tibia hemimelia in a patient with CHARGE syndrome: A rare but recurrent phenomenon.
Journal: American journal of medical genetics. Part A
Published: September 27, 2021
A guideline for the clinical management of basal cell naevus syndrome (Gorlin-Goltz syndrome).
Journal: The British journal of dermatology
Published: August 06, 2021
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD.
Journal: Journal of medical genetics
Published: September 12, 2019
Hypermobility in individuals with Kabuki syndrome: The effect of growth hormone treatment.
Journal: American journal of medical genetics. Part A
Published: July 19, 2018
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder.
Journal: American journal of human genetics
Published: February 14, 2018
A boy with digital clubbing
Journal: Nederlands tijdschrift voor geneeskunde
Published: January 06, 2018
Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.
Journal: European journal of human genetics : EJHG
Published: March 03, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026