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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1998 | 1 |
1999 | 3 |
2001 | 1 |
2024 | 0 |
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5 results
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Page 1
Frasier syndrome with childhood-onset renal failure.
Horm Res. 2001;55(2):77-80. doi: 10.1159/000049974.
Horm Res. 2001.
PMID: 11509863
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.
Waisfisz Q, Morgan NV, Savino M, de Winter JP, van Berkel CG, Hoatlin ME, Ianzano L, Gibson RA, Arwert F, Savoia A, Mathew CG, Pronk JC, Joenje H.
Waisfisz Q, et al.
Nat Genet. 1999 Aug;22(4):379-83. doi: 10.1038/11956.
Nat Genet. 1999.
PMID: 10431244
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Nuclear localization of the Fanconi anemia protein FANCC is required for functional activity.
Savoia A, Garcia-Higuera I, D'Andrea AD.
Savoia A, et al.
Blood. 1999 Jun 1;93(11):4025-6.
Blood. 1999.
PMID: 10383195
Free article.
No abstract available.
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Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.
Wijker M, Morgan NV, Herterich S, van Berkel CG, Tipping AJ, Gross HJ, Gille JJ, Pals G, Savino M, Altay C, Mohan S, Dokal I, Cavenagh J, Marsh J, van Weel M, Ortega JJ, Schuler D, Samochatova E, Karwacki M, Bekassy AN, Abecasis M, Ebell W, Kwee ML, de Ravel T, CG Mathew, et al.
Wijker M, et al.
Eur J Hum Genet. 1999 Jan;7(1):52-9. doi: 10.1038/sj.ejhg.5200248.
Eur J Hum Genet. 1999.
PMID: 10094191
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Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions.
Centra M, Memeo E, d'Apolito M, Savino M, Ianzano L, Notarangelo A, Liu J, Doggett NA, Zelante L, Savoia A.
Centra M, et al.
Genomics. 1998 Aug 1;51(3):463-7. doi: 10.1006/geno.1998.5353.
Genomics. 1998.
PMID: 9721219
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