Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1897-4287

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients ; volume:18 ; number:1 ; day:20 ; month:12 ; year:2020 ; pages:1-9 ; date:12.2020
Hereditary cancer in clinical practice ; 18, Heft 1 (20.12.2020), 1-9, 12.2020

Creator: Rashid, Muhammad Usman
Muhammad, Noor
Khan, Faiz Ali
Shehzad, Umara
Naeemi, Humaira
Malkani, Naila
Hamann, Ute

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13053-020-00159-6

URN: urn:nbn:de:101:1-2021020808221704993058

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:35 AM CEST

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Rashid, Muhammad Usman
Muhammad, Noor
Khan, Faiz Ali
Shehzad, Umara
Naeemi, Humaira
Malkani, Naila
Hamann, Ute
SpringerLink (Online service)

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Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

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Other Objects (12)

Correction to: Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

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A novel presenilin 1 mutation (Ala275Val) as cause of early-onset familial Alzheimer disease

BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients

BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia

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Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease

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Germline DNA copy number variation in familial and early-onset breast cancer

A comprehensive analysis of germline predisposition to early-onset ovarian cancer

Early-Onset Osteoporosis

Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

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BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients

BRCA1 mutations in women with familial or early-onset breast cancer and BRCA2 mutations in familial cancer in Estonia

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Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer

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