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Last Updated: 10/31/2025
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Found 65 publications
PTPN11 in cartilage development, adult homeostasis, and diseases.
Journal: Bone research
Published: January 24, 2025
The Cell-Specific Role of SHP2 in Regulating Bone Homeostasis and Regeneration Niches.
Journal: International journal of molecular sciences
Published: December 23, 2022
Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2.
Journal: Frontiers in cell and developmental biology
Published: September 16, 2022
Forearm Hereditary Multiple Exostosis: A Retrospective Case Series Study.
Journal: Cureus
Published: June 06, 2022
Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosis.
Journal: American journal of medical genetics. Part A
Published: June 03, 2021
Update on the imaging features of the enchondromatosis syndromes.
Journal: Skeletal radiology
Published: March 13, 2021
Metachondromatosis: A Confusing Disease.
Journal: Revista brasileira de ortopedia
Published: December 15, 2020
An unusual example of hereditary multiple exostoses: a case report and review of the literature.
Journal: BMC musculoskeletal disorders
Published: September 18, 2020
A rare association of pathological variant of Alport's syndrome caused by hemizygous 5' splice mutation in intron 10 of COL4A5 gene with metachondromatosis due to heterozygous missense variation in protein tyrosine phosphatase nonreceptor type 11 gene.
Journal: Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia
Published: August 30, 2019
Arthroscopic resection of femoral neck osteochondroma: Report of a pediatric case of metachondromatosis.
Journal: Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association
Published: April 23, 2019
Last Updated: 10/31/2025