Record title
Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8394758
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https://collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8394758
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Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
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Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
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England: BMJ Publishing Group LTD
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Journal of medical genetics, 2021, Vol.58 (9), p.648-652
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8394758
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English
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8394758
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https://collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8394758
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