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Nature Genetics|August 4, 1999
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicismQ Waisfisz, N V Morgan, M Savino, et al.Human Genetics|April 6, 2002
Identification of novel mutations in MLC1 responsible for megalencephalic leukoencephalopathy with subcortical cystsP A J Leegwater, P K I Boor, B Q Yuan, et al.American Journal of Human Genetics|April 17, 1999
The Fanconi anemia group E gene, FANCE, maps to chromosome 6pQ Waisfisz, K Saar, N V Morgan, et al.Stroke|August 28, 2004
Genome-wide linkage in a large Dutch consanguineous family maps a locus for intracranial aneurysms to chromosome 2p13Y B W E M Roos, G Pals, P M Struycken, et al.Nature Genetics|November 7, 1998
The Fanconi anaemia group G gene FANCG is identical with XRCC9J P de Winter, Q Waisfisz, M A Rooimans, et al.Genomics|February 26, 1999
The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancerJ Crawford, L Ianzano, M Savino, et al.American Journal of Human Genetics|March 20, 2001
Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cystsP A Leegwater, B Q Yuan, J van der Steen, et al.Nature Genetics|November 13, 2001
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matterP A Leegwater, G Vermeulen, A A Könst, et al.Genomics|May 1, 1997
The genomic organization of the Fanconi anemia group A (FAA) geneL Ianzano, M D'Apolito, M Centra, et al.Genomics|June 20, 1998
Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancerS A Whitmore, J Crawford, S Apostolou, et al.Pageof 7