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1 which is characterized by pulmonary vascular dysmorphia.
2 use and abuse, dieting regimens, and muscle dysmorphia.
3 diac abnormalities, short stature and facial dysmorphia.
4 triad of periodic paralysis, arrhythmia, and dysmorphia.
5 vimentin is involved in cancer cell nuclear dysmorphia.
6 cluding a likely AAS use disorder and muscle dysmorphia.
7 neurodevelopmental syndrome with mild facial dysmorphia.
8 iagnostic distinction based on the degree of dysmorphia.
9 een reported to have mild to moderate facial dysmorphia.
10 tal heart disease, short stature, and facial dysmorphia.
11 The authors interviewed 24 men with muscle dysmorphia and 30 normal comparison weightlifters, recru
14 easures, including marked symptoms of muscle dysmorphia and stronger endorsement of conventional male
15 e characterized by extremity anomalies, mild dysmorphia, and intellectual impairment caused by 3:1 me
16 n disorder, with short stature, craniofacial dysmorphia, and morphologic, histologic, echocardiograph
17 y will deeply phenotype cognition, behavior, dysmorphias, and neuromedical traits on an expected coho
19 s including cardiac abnormalities and facial dysmorphia but is not sufficient for tumor formation.
20 l defects such as growth delay, craniofacial dysmorphia, cardiac defects, and hematologic abnormaliti
24 cancer A549 cells largely prevented nuclear dysmorphia during the epithelial-to-mesenchymal transiti
25 asures but showed greater symptoms of muscle dysmorphia (e.g., not allowing their bodies to be seen i
27 , including growth delay, distinctive facial dysmorphia, hematologic abnormalities, and cardiac defec
30 rized by proportionate short stature, facial dysmorphia, increased risk of leukemia, and congenital h
34 individuals with DGS/VCFS, including: facial dysmorphia, mental retardation, long slender digits and
35 at unrestrained contractility causes nuclear dysmorphia, nuclear envelope rupture and genome instabil
37 ation) to phase III (inner retinal thinning, dysmorphia, pigment epithelium infiltration) remodeling.
39 scores on a retrospective adolescent muscle-dysmorphia scale, the hazard ratio was 1.5 (.84, 2.6); f
40 velopmental disorder characterized by facial dysmorphia, short stature, cardiac defects, and skeletal
44 velopmental disorder characterized by facial dysmorphia, upper limb malformations, growth and cogniti
45 velopmental disorder characterized by facial dysmorphia, upper-extremity malformations, hirsutism, ca
46 a novel role of VIFs in cancer cell nuclear dysmorphia, which is associated with genome instability.