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Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1–8 does not cause Beals syndrome |
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Titel: |
Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1–8 does not cause Beals syndrome |
Auteur: |
Maya, Idit Kahana, Sarit Agmon-Fishman, Ifaat Klein, Cochava Matar, Reut Berger, Racheli Shohat, Mordechai Basel-Salmon, Lina Sharony, Reuven Sagi-Dain, Lena |
Verschenen in: |
European journal of medical genetics |
Paginering: |
Jaargang 63 () nr. 10 pagina's p. |
Jaar: |
2020 |
Inhoud: |
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Uitgever: |
Elsevier Masson SAS |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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