BRCA1/2, PALB2 mutations in breast-ovarian syndrome, our series - BENCHOUK, Jesia Asma
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Breast cancer in Algeria, and more particularly in the western part of the country, has a particular epidemiological character which contrasts with universal data, due to its incidence in young and even very young patients in a historical context of multiple, multi-organ, transmissible family cancers.Our aim is to report on the overall history of index cases and related cases of breast-ovarian syndrome with BRCA1/BRCA2/PALB2 mutations in 38 young patients at the Sidi Bel Abbés Cancer Centre in Algeria.Our long-term objectives are to categorise the main genetic mutations and to develop a panel of genes specific to the different Algerian ethnic groups.…mehr

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Produktbeschreibung
Breast cancer in Algeria, and more particularly in the western part of the country, has a particular epidemiological character which contrasts with universal data, due to its incidence in young and even very young patients in a historical context of multiple, multi-organ, transmissible family cancers.Our aim is to report on the overall history of index cases and related cases of breast-ovarian syndrome with BRCA1/BRCA2/PALB2 mutations in 38 young patients at the Sidi Bel Abbés Cancer Centre in Algeria.Our long-term objectives are to categorise the main genetic mutations and to develop a panel of genes specific to the different Algerian ethnic groups.
Autorenporträt
Professor BENCHOUK Jesia Asma heads the breast and pelvic cancer surgery department at the Centre de Lutte Contre le Cancer in Sidi Bel Abbés, Algeria. She has also set up an oncogenetic consultation to screen for breast and ovarian cancers linked to family factors, given their early onset.