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Founder BRCA1 mutations in Nepalese population
Anurag Mehta, Himanshi Diwan, Garima Gupta, Shrinidhi Nathany, Shalini Agnihotri, Surender Dhanda
JPTM. 2022;56(4):212-216.   Published online 2022 June 15    DOI:

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Founder <i>BRCA1</i> mutations in Nepalese population
Journal of Pathology and Translational Medicine. 2022;56(4):212-216   Crossref logo
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Haplotype analysis of two recurrent genomic rearrangements in the BRCA1 gene suggests they are founder mutations for the Greek population
Clinical Genetics. 2010;80(4):375-382   Crossref logo
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High prevalence ofBRCA1founder mutations in Greek breast/ovarian families
Clinical Genetics. 2013;85(1):36-42   Crossref logo

The Features of BRCA1 and BRCA2 Germline Mutations in Hakka Ovarian Cancer Patients: BRCA1 C.536 A>T Maybe a Founder Mutation in This Population
International Journal of General Medicine. 2022;Volume 15:2773-2786   Crossref logo
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Prevalence of BRCA1 founder mutations in western Poland
Human Mutation. 2000;17(1):75-75   Crossref logo
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Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: A founder mutation of BRCA1 identified in the Chinese population
Human Mutation. 2002;19(3):307-308   Crossref logo
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BRCA1 founder mutations do not contribute to increased risk of gastric cancer in the Polish population
Hereditary Cancer in Clinical Practice. 2016;14(1):   Crossref logo
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Correction: Corrigendum: BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
Nature Genetics. 1997;17(4):503-503   Crossref logo
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Frequency of three BRCA1 gene founder mutations in breast/ovarian cancer families from the Pomerania-Kujawy region of Poland
Clinical Genetics. 2003;64(6):502-508   Crossref logo
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A low frequency of non-founder BRCA1 mutations in Ashkenazi Jewish breast-ovarian cancer families
Human Mutation. 2002;20(5):352-357   Crossref logo
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This metadata service is kindly provided by CrossRef from May 29, 2014. J Pathol Transl Med has participated in CrossRef Text and Data Mining service since January 16, 2015.