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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1990 | 1 |
1993 | 1 |
2001 | 1 |
2012 | 2 |
2024 | 0 |
PubMed for id: 1543388608
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ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome.
Nat Genet. 2012 May;44(5):575-80. doi: 10.1038/ng.2252.
Nat Genet. 2012.
PMID: 22522420
Free PMC article.
Congenital Muscular Dystrophy Overview – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY.
Sparks SE, Quijano-Roy S, Harper A, Rutkowski A, Gordon E, Hoffman EP, Pegoraro E.
Sparks SE, et al.
2001 Jan 22 [updated 2012 Aug 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
2001 Jan 22 [updated 2012 Aug 23]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID: 20301468
Free Books & Documents.
Review.
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Endotoxin in vivo impairs endothelium-dependent relaxation of canine arteries in vitro.
Wylam ME, Samsel RW, Umans JG, Mitchell RW, Leff AR, Schumacker PT.
Wylam ME, et al.
Am Rev Respir Dis. 1990 Dec;142(6 Pt 1):1263-7. doi: 10.1164/ajrccm/142.6_Pt_1.1263.
Am Rev Respir Dis. 1990.
PMID: 2252242
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