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/vufind/Search/Results?lookfor=%22Che%2C+Fengyu%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Che%2C+Fengyu%22&type=Person&sort=year
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PubPharm (33)
1
Correction to : Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
enthalten in:
Journal of applied genetics
| 2024
von
Che, F.
|
Li, C.
|
Zhang, L.
| +6
ErratumFor: J Appl Genet. 2024 May;65(2):367-373. - PMID 38418803
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2
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
enthalten in:
Journal of applied genetics
| 2024
von
Che, F.
|
Li, C.
|
Zhang, L.
| +6
ErratumIn: J Appl Genet. 2024 Mar 25;:. - PMID 38523169
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3
Correction to: Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
enthalten in:
Journal of applied genetics
| 2024
von
Che, F.
|
Li, C.
|
Zhang, L.
| +6
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4
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review
enthalten in:
Journal of applied genetics
| 2024
von
Che, F.
|
Li, C.
|
Zhang, L.
| +6
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5
A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35 : Genetic and Lipidomics Analysis of the Patients
enthalten in:
Pediatric neurology
| 2024
von
Mo, L.
|
Tie, X.
|
Che, F.
| +4
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6
Lethal variant in the C2A domain may cause severe SYT1-associated neurodevelopmental disorder in the newborns
enthalten in:
Neurogenetics
| 2024
von
Huang, W.
|
Yang, Y.
|
Che, F.
| +3
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7
Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient
enthalten in:
Stem cell research
| 2023
von
Li, B.
|
Zhou, Y.
|
Che, F.
| +5
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8
Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion : new clinical findings and genotype-phenotype correlations
enthalten in:
Molecular cytogenetics
| 2023
von
Zhang, L.
|
Tie, X.
|
Che, F.
| +4
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9
Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype–phenotype correlations
enthalten in:
Molecular cytogenetics
| 2023
von
Zhang, L.
|
Tie, X.
|
Che, F.
| +4
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10
Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype–phenotype correlations
enthalten in:
Molecular cytogenetics
| 2023
von
Zhang, L.
|
Tie, X.
|
Che, F.
| +4
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33
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Zhonghua yi xue yi chuan xue za zhi = Zhonghua ...
4
Journal of applied genetics
3
Frontiers in genetics
3
Molecular cytogenetics
2
Human mutation
2
International journal of nanomedicine
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Frontiers in molecular neuroscience
1
Journal of affective disorders
1
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Molecular therapy. Nucleic acids
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Pediatric neurology
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Thema
26
Journal Article
6
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4
Aptamers, Nucleotide
4
Research Support, Non-U.S. Gov't
2
Antineoplastic Agents
2
FARS2
2
Genotype and phenotype
2
Interleukin-3
2
Interleukin-3 Receptor alpha Subunit
2
Published Erratum
2
Purkinje cells
2
Speech-language disorder
2
Transcription Factors
2
aptamer
2
hereditary spastic paraplegia
2
molecular diagnosis
2
neurodegenerative disorder
1
01K63SUP8D
1
104982-03-8
1
3-Oxo-5-alpha-Steroid 4-Dehydrogenase
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Erscheinungszeitraum
28
2020-
5
2010-2019
Erscheinungsjahr(e)
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Sprache
24
Englisch
9
Chinesisch
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