Correction to: Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1897-4287
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Correction to: Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients ; volume:19 ; number:1 ; day:7 ; month:1 ; year:2021 ; pages:1-2 ; date:12.2021
Hereditary cancer in clinical practice ; 19, Heft 1 (7.1.2021), 1-2, 12.2021
- Klassifikation
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Medizin, Gesundheit
- Urheber
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Rashid, Muhammad Usman
Muhammad, Noor
Khan, Faiz Ali
Shehzad, Umara
Naeemi, Humaira
Malkani, Naila
Hamann, Ute
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13053-020-00163-w
- URN
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urn:nbn:de:101:1-2021020804061601287403
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:38 MESZ
Datenpartner
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Beteiligte
- Rashid, Muhammad Usman
- Muhammad, Noor
- Khan, Faiz Ali
- Shehzad, Umara
- Naeemi, Humaira
- Malkani, Naila
- Hamann, Ute
- SpringerLink (Online service)
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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
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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
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Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease
Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients
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
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BRCA mutations: screening for germ-line founder mutations among early-onset Syrian breast cancer patients
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