Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Emmanuel T, Aladenika"'
Autor:
Waheed, Awotoye, Peter A, Mossey, Jacqueline B, Hetmanski, Lord J J, Gowans, Mekonen A, Eshete, Wasiu L, Adeyemo, Azeez, Alade, Erliang, Zeng, Olawale, Adamson, Olutayo, James, Azeez, Fashina, Modupe O, Ogunlewe, Thirona, Naicker, Chinyere, Adeleke, Tamara, Busch, Mary, Li, Aline, Petrin, Abimbola, Oladayo, Sami, Kayali, Joy, Olotu, Veronica, Sule, Mohaned, Hassan, John, Pape, Emmanuel T, Aladenika, Peter, Donkor, Fareed K N, Arthur, Solomon, Obiri-Yeboah, Daniel K, Sabbah, Pius, Agbenorku, Debashree, Ray, Gyikua, Plange-Rhule, Alexander Acheampong, Oti, Daniah, Albokhari, Nara, Sobreira, Martine, Dunnwald, Terri H, Beaty, Margaret, Taub, Mary L, Marazita, Adebowale A, Adeyemo, Jeffrey C, Murray, Azeez, Butali
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
Novel or rare damaging mutations have been implicated in the developmental pathogenesis of nonsyndromic cleft lip with or without cleft palate (nsCL ± P). Thus, we investigated the human genome for high-impact mutations that could explain the risk o
Damaging Mutations in AFDN Contribute to Risk of Nonsyndromic Cleft Lip With or Without Cleft Palate
Autor:
Waheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, Lord J J Gowans, Mekonen A Eshete, Wasiu L Adeyemo, Azeez Alade, Erliang Zeng, Olawale Adamson, Olutayo James, Azeez Fashina, Modupe O Ogunlewe, Thirona Naicker, Chinyere Adeleke, Tamara Busch, Mary Li, Aline Petrin, Abimbola Oladayo, Sami Kayali, Joy Olotu, Veronica Sule, Mohaned Hassan, John Pape, Emmanuel T Aladenika, Peter Donkor, Fareed K N Arthur, Solomon Obiri-Yeboah, Daniel K Sabbah, Pius Agbenorku, Debashree Ray, Gyikua Plange-Rhule, Alexander Acheampong Oti, Daniah Albokhari, Nara Sobreira, Martine Dunnwald, Terri H Beaty, Margaret Taub, Mary L Marazita, Adebowale A Adeyemo, Jeffrey C Murray, Azeez Butali
Publikováno v:
The Cleft Palate-Craniofacial Journal. :105566562211359
Novel or rare damaging mutations have been implicated in the developmental pathogenesis of nonsyndromic cleft lip with or without cleft palate (nsCL ± P). Thus, we investigated the human genome for high-impact mutations that could explain the risk o