Zobrazeno 1 - 5
of 5
pro vyhledávání: '"I M, Mazen"'
Autor:
H H, Afifi, M O, El-Ruby, H T, El-Bassyouni, S I, Ismail, M S, Aglan, A A, El-Harouni, I M, Mazen, M S, Zaki, R I, Bassiouni, L A, Hosny, G Y, El-Kamah, A I, El-Kotoury, A M, Ashour, G M, Abdel-Salam, M A, El-Gammal, K, Hamed, R M, Kamal, I, El-Nekhely, S A, Temtamy
Publikováno v:
Bratislavske lekarske listy. 111(2)
This study presents the prevalence, relative frequency, and analysis of genetic diseases/malformations in 73260 individuals. Cases included were ascertained from: Pediatric outpatient clinics of two governmental hospitals and two primary health care
Publikováno v:
Genetic counseling (Geneva, Switzerland). 16(1)
Ellis-van Creveld (EVC) syndrome (chondroectodermal dysplasia, mesoectodermal dysplasia, OMIM 225500) is an autosomal recessive skeletal dysplasia characterized by short limbs, short ribs, postaxial polydactyly and dysplastic nails and teeth. Oral ma
Autor:
Al-Khatib, M.M., Bayoumi, M.
Publikováno v:
WCNC 1999 IEEE Wireless Communications & Networking Conference (Cat No99TH8466); 1999, Issue 3, p1407-1407, 1p
Autor:
Kouri, Chrysanthi, Sommer, Grit, Ahmed, Faisal, Balsamo, Antonio, Baronio, Federico, Bryce, Jillian, Camats, Nuria, Cetinkaya, Semra, Hedi L. Claahsen - van der Grinten, Cools, Martine, Darendeliler, Fatma Feyza, Davies, Justin H., Fabbri-Scallet, Helena, Globa, Evgenia, Guerra-Junior, Gil, Guran, Tulay, Hannema, Sabine, Hiort, Olaf, Janner, Marco, Kalinchenko, Natalia, Lachlan, Katherine, Kolesinska, Zofia, L Allemand, Dagmar, Lang-Muritano, Mariarosaria, Lucas-Herald, Angela, Lapiscina Martin, Idoia Martinez, Mazen, Inas, Moenig, Isabel, Muhrer, Julia, Niedziela, Marek, Nordenstrom, Anna, Orman, Burce, Poyrazoglu, Sukran, Tack, Lloyd, Tadokoro-Cuccaro, Rieko, Wasniewska, Malgorzata, Yavas, Zehra, Zelinska, Nataliya, Fluck, Christa E.
Publikováno v:
Web of Science
Kouri, C, Sommer, G, Ahmed, F, Balsamo, A, Baronio, F, Bryce, J, Camats, N, Cetinkaya, S, Claahsen-van der Grinten, H L, Cools, M, Darendeliler, F F, Davies, J H, Fabbri-Scallet, H, Globa, E, Guerra-Junior, G, Guran, T, Hannema, S, Hiort, O, Janner, M, Kalinchenko, N, Lachlan, K, Kolesinska, Z, l'Allemand, D, Lang-Muritano, M, Lucas-Herald, A, de Lapiscina Martin, I M, Mazen, I, Moenig, I, Muhrer, J, Niedziela, M, Nordenstrom, A, Orman, B, Poyrazoglu, S, Tack, L, Tadokoro-Cuccaro, R, Wasniewska, M, Yavas, Z, Zelinska, N & Fluck, C E 2021, ' Broad range of phenotypes in an international cohort of 75 DSD individuals with SF-1/NR5A1 variants ', Hormone Research in Paediatrics, vol. 94, no. SUPPL 1, pp. 87-89 .
Hormone Research in Paediatrics, 94(SUPPL 1), 87-89. S. Karger AG
Kouri, C, Sommer, G, Ahmed, F, Balsamo, A, Baronio, F, Bryce, J, Camats, N, Cetinkaya, S, Claahsen-van der Grinten, H L, Cools, M, Darendeliler, F F, Davies, J H, Fabbri-Scallet, H, Globa, E, Guerra-Junior, G, Guran, T, Hannema, S, Hiort, O, Janner, M, Kalinchenko, N, Lachlan, K, Kolesinska, Z, l'Allemand, D, Lang-Muritano, M, Lucas-Herald, A, de Lapiscina Martin, I M, Mazen, I, Moenig, I, Muhrer, J, Niedziela, M, Nordenstrom, A, Orman, B, Poyrazoglu, S, Tack, L, Tadokoro-Cuccaro, R, Wasniewska, M, Yavas, Z, Zelinska, N & Fluck, C E 2021, ' Broad range of phenotypes in an international cohort of 75 DSD individuals with SF-1/NR5A1 variants ', Hormone Research in Paediatrics, vol. 94, no. SUPPL 1, pp. 87-89 .
Hormone Research in Paediatrics, 94(SUPPL 1), 87-89. S. Karger AG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::685813e978a8bfb3ded0e3cac2defb4c
https://publons.com/wos-op/publon/50069806/
https://publons.com/wos-op/publon/50069806/
Autor:
Robert E. Davis
'A much-needed service for society today. I hope this book reaches information managers in the organization now vulnerable to hacks that are stealing corporate information and even holding it hostage for ransom.'– Ronald W. Hull, author, poet, and