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1 Ergebnisse
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Combining RSPH9 founder mutation screening and next-generat..:
Mabrouk, Imed
;
Al-Harthi, Nawal
;
Mani, Rahma
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s10038-021-01006-9. , 2022
Link:
https://hal.sorbonne-universite.fr/hal-03551986
RT Journal T1
Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients
UL https://suche.suub.uni-bremen.de/peid=base-ftccsdartic:oai:HAL:hal-03551986v1&Exemplar=1&LAN=DE A1 Mabrouk, Imed A1 Al-Harthi, Nawal A1 Mani, Rahma A1 Montantin, Guy A1 Tissier, Sylvie A1 Lagha, Rihab A1 Ben Abdallah, Fethi A1 Hassan, Mohamad, M A1 Alhomrani, Majid A1 Gaber, Ahmed A1 Alsanie, Walaa, F A1 Ouali, Hanadi A1 Jambi, Fatma, A A1 Almaghamsi, Talal, M A1 Alqarni, Nawal, A A1 Alfarsi, Nawaf, A A1 Kashgari, Khadija A1 Al-Zahrani, Hasna, J A1 Al-Shamary, Zamel, A A1 Al-Harbi, Abdullah A1 Amselem, Serge A1 Escudier, Estelle A1 Legendre, Marie PB HAL CCSD; Nature Publishing Group YR 2022 K1 [SDV.GEN]Life Sciences [q-bio]/Genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1038/s10038-021-01006-9 LK http://dx.doi.org/https://hal.sorbonne-universite.fr/hal-03551986 DO https://hal.sorbonne-universite.fr/hal-03551986 SF ELIB - SuUB Bremen
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