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Year | Number of Results |
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2007 | 3 |
2015 | 1 |
2024 | 0 |
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Page 1
Identification of Critical Region Responsible for Split Hand/Foot Malformation Type 3 (SHFM3) Phenotype through Systematic Review of Literature and Mapping of Breakpoints Using Microarray Data.
Microarrays (Basel). 2015 Dec 24;5(1):2. doi: 10.3390/microarrays5010002.
Microarrays (Basel). 2015.
PMID: 27600068
Free PMC article.
Prenatally diagnosed mosaic trisomy 14q with omphalocele.
Wang JC, Li CF, Shaw DR.
Wang JC, et al. Among authors: li cf.
Prenat Diagn. 2007 Dec;27(13):1260-1. doi: 10.1002/pd.1880.
Prenat Diagn. 2007.
PMID: 17994633
No abstract available.
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Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse.
Li CF, MacDonald JR, Wei RY, Ray J, Lau K, Kandel C, Koffman R, Bell S, Scherer SW, Alman BA.
Li CF, et al.
BMC Genomics. 2007 Apr 3;8:92. doi: 10.1186/1471-2164-8-92.
BMC Genomics. 2007.
PMID: 17407603
Free PMC article.
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An association between the 4G polymorphism in the PAI-1 promoter and the development of aggressive fibromatosis (desmoid tumor) in familial adenomatous polyposis patients.
Li CF, Wei RY, Baliko F, Bapat B, Alman BA.
Li CF, et al.
Fam Cancer. 2007;6(1):89-95. doi: 10.1007/s10689-006-9109-5.
Fam Cancer. 2007.
PMID: 17160433
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