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/vufind/Search/Results?lookfor=%22Hu%2C+Ping%22&type=Person&filter%5B%5D=topic_facet%3A%22Case+Reports%22
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PubPharm (35)
1
A case of giant unruptured aneurysms of the sinuses of Valsalva
enthalten in:
Echocardiography (Mount Kisco, N.Y.)
| 2024
von
Song, Q.
|
Ma, X.
|
Xia, J.
| +2
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2
11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four-way balanced chromosomal translocation
enthalten in:
Molecular genetics & genomic medicine
| 2023
von
Zhang, Q.
|
Wang, Y.
|
Zhou, J.
| +6
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3
Whole genome sequencing vs chromosomal microarray analysis in prenatal diagnosis
enthalten in:
American journal of obstetrics and gynecology
| 2023
von
Hu, P.
|
Zhang, Q.
|
Cheng, Q.
| +9
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4
Genetic analysis of a fetus with mosaic trisomy 12 and severe heart defects and a literature review
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2023
von
Yin, T.
|
Wang, Z.
|
Tan, J.
| +4
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5
Case report : Uncommon multiple metastases from occult breast cancer revealed by 68Ga-DOTATATE PET/CT
enthalten in:
Frontiers in oncology
| 2023
von
Hu, T.
|
Zhang, R.
|
Zhang, B.
| +7
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6
A rare coronary anomaly : The single left coronary artery with coronary artery fistula draining into the right ventricular outflow tract
enthalten in:
Echocardiography (Mount Kisco, N.Y.)
| 2023
von
Wang, J.
|
Hu, P.
|
Ku, L.
| +2
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7
Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiency
enthalten in:
Journal of clinical laboratory analysis
| 2022
von
Zhang, J.
|
Ma, D.
|
Liu, G.
| +5
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8
Proline-rich transmembrane protein 2 specifically binds to GluA1 but has no effect on AMPA receptor-mediated synaptic transmission
enthalten in:
Journal of clinical laboratory analysis
| 2022
von
Feng, H.
|
Qiao, F.
|
Tan, J.
| +4
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9
Case Report : Dual-Energy Computed Tomography of Cardiac Changes in IgG4-Related Disease
enthalten in:
Frontiers in cardiovascular medicine
| 2022
von
Wang, Y.
|
Zhou, H.
|
Hu, P.
| +4
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10
Case Report : Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome
enthalten in:
Frontiers in genetics
| 2021
von
Qiao, F.
|
Zhang, C.
|
Wang, Y.
| +4
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Thema: Case Reports
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35
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Case Reports
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intellectual disability
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