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Hypotonia

Adverse events following Synflorix vaccination reported to the Vaccine Adverse Event Reporting System (VAERS), 2010–2024

Lingyun Cui, Nian Tong, Sicong Hou, Chun Yu

New genes involved in Angelman syndrome-like: Expanding the genetic spectrum

Cinthia Aguilera, Elisabeth Gabau, [ ... ], Anna Ruiz

Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability

Christina Grau, Molly Starkovich, [ ... ], Daryl A. Scott

Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex

Saketh Kapoor, Mohd Hussain Shah, [ ... ], Arun Kumar

Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome

Kaihui Zhang, Shu Liu, [ ... ], Zhongtao Gai

MeCP2 Affects Skeletal Muscle Growth and Morphology through Non Cell-Autonomous Mechanisms

Valentina Conti, Anna Gandaglia, [ ... ], Nicoletta Landsberger

Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy

Dandan Tan, Haipo Yang, [ ... ], Hui Xiong

Deletion of Prepl Causes Growth Impairment and Hypotonia in Mice

Anna Mari Lone, Mathias Leidl, [ ... ], Alan Saghatelian

Mechanisms of Esophago-Pharyngeal Acid Regurgitation in Human Subjects

Michal Marcin Szczesniak, Rohan Benjamin Williams, Ian James Cook

Histology of the Pharyngeal Constrictor Muscle in 22q11.2 Deletion Syndrome and Non-Syndromic Children with Velopharyngeal Insufficiency

Josine C. C. Widdershoven, Nicole E. Spruijt, [ ... ], Aebele B. Mink van der Molen

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