
Last Updated: 09/26/2026
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Found 38 publications
Identification of Modified Histones as Binding Substrates of Human Spindlin Family Member 4 (SPIN4) by Peptide Arrays and Native Nucleosome Pulldown.
Journal: Journal of visualized experiments : JoVE
Published: April 13, 2026
International guideline on genetic testing of children with short stature.
Journal: European journal of endocrinology
Published: January 03, 2026
Novelty Detection for Bone Age Anomaly Identification Using Self-Supervised Learning.
Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference
Published: December 03, 2025
Phalangeal bone growth and implications in Turner syndrome.
Journal: Frontiers in endocrinology
Published: October 30, 2025
SPIN4-related X-linked overgrowth in a family.
Journal: European journal of medical genetics
Published: September 10, 2025
A Novel Variant in an Intron Splicing Enhancer Associated with Familial Growth Hormone Deficiency.
Journal: Hormone research in paediatrics
Published: August 14, 2024
Variants in WASHC3, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphism.
Journal: Genetics in medicine open
Published: May 22, 2024
Persistent Gynecomastia due to Short-term Low-dose Finasteride for Androgenetic Alopecia.
Journal: JCEM case reports
Published: January 16, 2024
The Association of Accelerated Early Growth, Timing of Puberty, and Metabolic Consequences in Children.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 12, 2023
Loss-of-function variant in SPIN4 causes an X-linked overgrowth syndrome.
Journal: JCI insight
Published: November 11, 2022
Understanding Prenatal and Postnatal Linear Growth.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 12, 2022
Last Updated: 09/26/2026