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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 1 |
2011 | 2 |
2021 | 1 |
2022 | 2 |
2024 | 0 |
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Page 1
Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature.
J Med Genet. 2010 Apr;47(4):281-7. doi: 10.1136/jmg.2009.070565.
J Med Genet. 2010.
PMID: 20413710
Free PMC article.
Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome.
Benhammou JN, Vocke CD, Santani A, Schmidt LS, Baba M, Seyama K, Wu X, Korolevich S, Nathanson KL, Stolle CA, Linehan WM.
Benhammou JN, et al.
Genes Chromosomes Cancer. 2011 Jun;50(6):466-77. doi: 10.1002/gcc.20872. Epub 2011 Mar 15.
Genes Chromosomes Cancer. 2011.
PMID: 21412933
Free PMC article.
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Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families.
Houweling AC, Gijezen LM, Jonker MA, van Doorn MB, Oldenburg RA, van Spaendonck-Zwarts KY, Leter EM, van Os TA, van Grieken NC, Jaspars EH, de Jong MM, Bongers EM, Johannesma PC, Postmus PE, van Moorselaar RJ, van Waesberghe JH, Starink TM, van Steensel MA, Gille JJ, Menko FH.
Houweling AC, et al.
Br J Cancer. 2011 Dec 6;105(12):1912-9. doi: 10.1038/bjc.2011.463.
Br J Cancer. 2011.
PMID: 22146830
Free PMC article.
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A Novel FLCN Intragenic Deletion Identified by NGS in a BHDS Family and Literature Review.
Cai M, Zhang X, Fan L, Cheng S, Kiram A, Cen S, Chen B, Ye M, Gao Q, Zhu C, Yi L, Ma D.
Cai M, et al.
Front Genet. 2021 Apr 1;12:636900. doi: 10.3389/fgene.2021.636900. eCollection 2021.
Front Genet. 2021.
PMID: 33927747
Free PMC article.
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Clinical and Genetic Comparison of Birt-Hogg-Dubé Syndrome (Hornstein-Knickenberg Syndrome) in Chinese: A Systemic Review of Reported Cases.
Zhou W, Liu K, Xu KF, Liu Y, Tian X.
Zhou W, et al.
Int J Gen Med. 2022 May 23;15:5111-5121. doi: 10.2147/IJGM.S359660. eCollection 2022.
Int J Gen Med. 2022.
PMID: 35637701
Free PMC article.
Review.
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Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system population.
Savatt JM, Shimelis H, Moreno-De-Luca A, Strande NT, Oetjens MT, Ledbetter DH, Martin CL, Myers SM, Finucane BM.
Savatt JM, et al.
Genet Med. 2022 Sep;24(9):1857-1866. doi: 10.1016/j.gim.2022.05.006. Epub 2022 May 31.
Genet Med. 2022.
PMID: 35639097
Free PMC article.
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