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Medientyp
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Autor/in
- Hisama, Fuki M
- Lessel, Davor 7
- Saha, Bidisha 5
- Kubisch, Christian 3
- Martin, George M 3
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Sprache
- Englisch 7
7 Einträge gefunden
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CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures
- Sargolzaeiaval, Forough
- Zhang, Jiaming
- Schleit, Jennifer
- Lessel, Davor
- Kubisch, Christian
- Precioso, Debora R
- Sillence, David
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Dysfunction of the MDM2/p53 axis is linked to premature aging
- Lessel, Davor
- Wu, Danyi
- Trujillo, Carlos
- Ramezani, Thomas
- Lessel, Ivana
- Alwasiyah, Mohammad K
- Saha, Bidisha
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WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.
- Yokote, Koutaro
- Chanprasert, Sirisak
- Lee, Lin
- Eirich, Katharina
- Takemoto, Minoru
- Watanabe, Aki
- Koizumi, Naoko
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POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome
- Lessel, Davor
- Hisama, Fuki M
- Szakszon, Katalin
- Saha, Bidisha
- Sanjuanelo, Alexander Barrios
- Salbert, Bonnie A
- Steele, Pamela D
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Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry
- Saha, Bidisha
- Lessel, Davor
- Nampoothiri, Sheela
- Rao, Anuradha S
- Hisama, Fuki M
- Peter, Dincy
- Bennett, Chris
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