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A unique case of progressive hemifacial microsomia or Parry..:
Pattnaik, Anandita
;
Lim, Alexandra
;
Sabeti, Sara
...
qt2dx1m6fs. , 2021
Link:
https://escholarship.org/uc/item/2dx1m6fs
RT Journal T1
A unique case of progressive hemifacial microsomia or Parry-Romberg syndrome associated with limb and brain anomalies with normal neurological findings: A review of the literature
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt2dx1m6fs&Exemplar=1&LAN=DE A1 Pattnaik, Anandita A1 Lim, Alexandra A1 Sabeti, Sara A1 Kwon, Ashley A1 Hall, Katherine A1 Lott, Ira A1 Kimonis, Virginia PB eScholarship, University of California YR 2021 K1 Biomedical and Clinical Sciences K1 Clinical Sciences K1 Congenital Structural Anomalies K1 Neurodegenerative K1 Pain Research K1 Biomedical Imaging K1 Clinical Research K1 Pediatric K1 Neurosciences K1 Chronic Pain K1 Aetiology K1 2.1 Biological and endogenous factors K1 Neurological K1 Brain K1 Child K1 Facial Hemiatrophy K1 Female K1 Goldenhar Syndrome K1 Humans K1 Limb Deformities K1 Congenital K1 Phenotype K1 Parry-Romberg syndrome K1 Hemifacial atrophy K1 Midline indentation K1 White matter lesions K1 Genetics K1 Genetics & Heredity JF qt2dx1m6fs LK http://dx.doi.org/https://escholarship.org/uc/item/2dx1m6fs DO https://escholarship.org/uc/item/2dx1m6fs SF ELIB - SuUB Bremen
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