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/vufind/Search/Results?lookfor=%22Robson%2C+Caroline+D.%22&type=Person&sort=year
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PubPharm (172)
1
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders
enthalten in:
bioRxiv.org
| 2024
von
Jurgens, J.
|
Barry, B.
|
Chan, W.
| +37
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2
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders
enthalten in:
medRxiv : the preprint server for health sciences
| 2024
von
Jurgens, J.
|
Barry, B.
|
Chan, W.
| +38
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3
A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder
enthalten in:
Genetics in medicine : official journal of the American College of Medical Genetics
| 2024
von
Lecoquierre, F.
|
Punt, A.
|
Ebstein, F.
| +28
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4
Single-institution Series of Hirayama Disease in North America
enthalten in:
Clinical spine surgery
| 2024
von
Lynch, B.
|
Slingerland, A.
|
Robson, C.
| +4
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5
CTNNB1 and APC Mutations in Sinonasal Myxoma : Expanding the Spectrum of Tumors Driven By WNT/β-catenin Pathway
enthalten in:
The American journal of surgical pathology
| 2023
von
Chen, S.
|
Gallant, S.
|
Cunningham, M.
| +4
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6
Non-Syndromic Sensorineural Hearing Loss in Children
enthalten in:
Neuroimaging clinics of North America
| 2023
von
Robson, C.
|
Lewis, M.
|
D'Arco, F.
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7
Conductive Hearing Loss in Children
enthalten in:
Neuroimaging clinics of North America
| 2023
von
Robson, C.
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8
Syndromic Hearing Loss in Children
enthalten in:
Neuroimaging clinics of North America
| 2023
von
Lewis, M.
|
Robson, C.
|
D'Arco, F.
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9
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis
enthalten in:
Nature genetics
| 2023
von
Tenney, A.
|
Di Gioia, S.
|
Webb, B.
| +55
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10
A multi-disciplinary team approach to pediatric malignant mandibular tumors
enthalten in:
International journal of pediatric otorhinolaryngology
| 2023
von
Hintze, J.
|
Afshar, S.
|
Taghinia, A.
| +7
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7
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5
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4
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4
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4
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