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BRCA2 T2722R Is a Deleterious Allele That Causes Exon Skipping - ScienceDirect
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Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundary - Whiley - 2011 - Human Mutation - Wiley Online Library
Transcription of CLDND1 in human brain endothelial cells is regulated by the myeloid zinc finger 1 - Shima - 2021 - Clinical and Experimental Pharmacology and Physiology - Wiley Online Library
Characterization of three alternative transcripts of the BRCA1 gene in patients with breast cancer and a family history of breast and/or ovarian cancer who tested negative for pathogenic mutations
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Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma | PNAS
Report BRCA2 T2722R Is a Deleterious Allele That Causes Exon Skipping
Family D in whom deletion of exon 20 of the BRCA1 gene was detected. a.... | Download Scientific Diagram
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BRCA2 T2722R is a deleterious allele that causes exon skipping. - Abstract - Europe PMC
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Pictorial representation of a genomic fragment (5 to 3 ) showing... | Download Scientific Diagram
