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PubPharm (53)
1
Biallelic truncating TTN variants in M-band encoding exons cause a fetal lethal titinopathy
enthalten in:
Prenatal diagnosis
| 2024
von
Li, M.
|
Li, F.
|
Cheng, Z.
| +5
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2
Pitfalls in diagnosing a case of extranodal NK/T-cell lymphoma with CD20 aberrant expression and IGH gene rearrangement
enthalten in:
Journal of cutaneous pathology
| 2023
von
Liu, C.
|
Li, F.
|
Mao, C.
| +2
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3
Primary spindle cell tumor with branching blood vessels of the neck : A case report
enthalten in:
Asian journal of surgery
| 2023
von
Liang, Y.
|
Zhang, P.
|
Li, F.
| +1
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4
Varicella-zoster virus meningitis with hypoglycorrhachia : A case report
enthalten in:
World journal of clinical cases
| 2023
von
Cao, L.
|
Zheng, Y.
|
Li, F.
| +2
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5
A case of Marine Lenhart syndrome with Hashimoto's thyroiditis that mimicked thyroid carcinoma
enthalten in:
BMC endocrine disorders
| 2023
von
Ye, P.
|
Li, L.
|
Wei, D.
| +3
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6
Rare Pattern of Myelodysplastic Syndrome (MDS) with Serum Monoclonal Immunoglobulin : Case Report
enthalten in:
Alternative therapies in health and medicine
| 2023
von
Lin, Y.
|
He, J.
|
Li, F.
| +1
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7
Real-World COPD Management Over 3 Years at the Community Health Service Center of Shanghai During the COVID-19 Pandemic in China
enthalten in:
International journal of chronic obstructive pulmonary disease
| 2023
von
Wu, T.
|
Jiang, Y.
|
Zhao, B.
| +7
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8
Aplastic crisis induced by human parvovirus B19 infection in a previously healthy adult male : A case report
enthalten in:
Asian journal of surgery
| 2022
von
Lin, Y.
|
Ding, G.
|
Li, F.
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9
A rare case of 48, XXYY syndrome in Taiwan
enthalten in:
Pediatrics and neonatology
| 2022
von
Pai, L.
|
Wang, D.
|
Chu, D.
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10
Recurrent Androgenetic Complete Hydatidiform Moles with p57KIP2-Positive in a Chinese Family
enthalten in:
Reproductive sciences (Thousand Oaks, Calif.)
| 2022
von
Li, M.
|
Li, F.
|
Cheng, J.
| +2
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Thema: Case Reports
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53
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Thema
Case Reports
38
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10
Research Support, Non-U.S. Gov't
6
Letter
5
0Z5B2CJX4D
5
Fluorodeoxyglucose F18
5
Review
3
Case report
2
immunohistochemistry
1
10q22.2q22.3 deletion
1
3XMK78S47O
1
4G7DS2Q64Y
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4TI98Z838E
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4Z8R6ORS6L
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56320-22-0
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7S5I7G3JQL
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8001-22-7
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971Z4W1S09
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Alexander disease
1
Androgenetic uniparental disomy
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Erscheinungszeitraum
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2010-2019
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2000-2009
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