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Genes | Free Full-Text | The Importance of Extended Analysis Using Current Molecular Genetic Methods Based on the Example of a Cohort of 228 Patients with Hereditary Breast and Ovarian Cancer Syndrome | HTML
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Altered regulation of BRCA1 exon 11 splicing is associated with breast cancer risk in carriers of BRCA1 pathogenic variants - Ruiz de Garibay - 2021 - Human Mutation - Wiley Online Library
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IJMS | Free Full-Text | Novel Nine-Exon AR Transcripts (Exon 1/Exon 1b/Exons 2–8) in Normal and Cancerous Breast and Prostate Cells | HTML
Gene trapping identifies chloride channel 4 as a novel inducer of colon cancer cell migration, invasion and metastases | British Journal of Cancer
BRCA2 T2722R is a deleterious allele that causes exon skipping. - Abstract - Europe PMC
Report BRCA2 T2722R Is a Deleterious Allele That Causes Exon Skipping
Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families | Oncogene
BRCA2 T2722R Is a Deleterious Allele That Causes Exon Skipping - ScienceDirect
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
Altered regulation of BRCA1 exon 11 splicing is associated with breast cancer risk in carriers of BRCA1 pathogenic variants - Ruiz de Garibay - 2021 - Human Mutation - Wiley Online Library
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Genetic Counseling, Testing, and Management of HBOC in India: An Expert Consensus Document from Indian Society of Medical and Pediatric Oncology | JCO Global Oncology
Family D in whom deletion of exon 20 of the BRCA1 gene was detected. a.... | Download Scientific Diagram
Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma | PNAS
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