Results 221 to 230 of about 509,989 (407)
ABSTRACT Apert syndrome is a recognizable craniofacial condition characterized by craniosynostosis, hypertelorism, exorbitism, midface hypoplasia, and complex symmetrical bony and cutaneous ‘mitten’ syndactyly of all four limbs. Around 98% of affected patients have one of two heterozygous missense variants in the FGFR2 gene, encoding either p ...
Ramy Saad +8 more
wiley +1 more source
Forearm Rotation at the Time of Elbow Ulnar Collateral Ligament Reconstruction Graft Tensioning Does Not Affect Postoperative Medial Elbow Joint Gapping. [PDF]
Selley RS +5 more
europepmc +1 more source
Forearm Positioning on Maximal Elbow-flexor Force [PDF]
Robert F. Larson
openalex +1 more source
Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato +2 more
wiley +1 more source
Postoperative Outcomes of Anteromedial Approach in Patients with Elbow Varus Posteromedial Rotatory Instability: A Retrospective Study. [PDF]
Huang H +5 more
europepmc +1 more source
TRUE ANCHYLOSIS OF BOTH ELBOWS IN A NEARLY EXTENDED POSITION, IN WHICH RESECTION WAS PERFORMED ON THE LEFT. [PDF]
C. Holthouse
openalex +1 more source
Tendinitis Calcarea of the Extensor Origin at the Elbow with Effusion of the Joint [PDF]
W. J. Weston
openalex +1 more source
ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen +10 more
wiley +1 more source

