Zobrazeno 1 - 10
of 16 432
pro vyhledávání: '"genetic disorder"'
Autor:
Müller, Annelieke R.1,2,3,4 (AUTHOR), Boot, Erik4,5,6 (AUTHOR), Notermans, Stijn B.1 (AUTHOR), Schuengel, Carlo3,7 (AUTHOR), Henneman, Lidewij8,9 (AUTHOR), Cornel, Martina C.3,8,9 (AUTHOR), van Haelst, Mieke M.9,10 (AUTHOR), Alders, Mariëlle9,10 (AUTHOR), van Karnebeek, Clara D. M.1,2,10 (AUTHOR), Bijl, Bas4 (AUTHOR), Wijburg, Frits A.1 (AUTHOR), van Eeghen, Agnies M.2,3,4,9 (AUTHOR) a.m.vaneeghen@amsterdamumc.nl
Publikováno v:
Orphanet Journal of Rare Diseases. 9/16/2024, Vol. 19 Issue 1, p1-11. 11p.
Autor:
Perinelli, Martina Giorgia1 (AUTHOR), Abbott, Megan2,3 (AUTHOR), Balagura, Ganna1 (AUTHOR), Riva, Antonella1 (AUTHOR), Amadori, Elisabetta4 (AUTHOR), Verrotti, Alberto5 (AUTHOR), Demarest, Scott2,3 (AUTHOR), Striano, Pasquale1,4 (AUTHOR) pasqualestriano@gaslini.org
Publikováno v:
Systematic Reviews. 8/31/2024, Vol. 13 Issue 1, p1-6. 6p.
Autor:
Fernández-Suárez, Elena1,2 (AUTHOR), González-del Pozo, María1,2 (AUTHOR), Méndez-Vidal, Cristina1,2 (AUTHOR), Martín-Sánchez, Marta1,2 (AUTHOR), Mena, Marcela1,2 (AUTHOR), de la Morena-Barrio, Belén3 (AUTHOR), Corral, Javier3 (AUTHOR), Borrego, Salud1,2 (AUTHOR) salud.borrego.sspa@juntadeandalucia.es, Antiñolo, Guillermo1,2 (AUTHOR) gantinolo@us.es
Publikováno v:
Mobile DNA. 5/4/2024, Vol. 15 Issue 1, p1-12. 12p.
Autor:
Webb, Bryn D.1,2 (AUTHOR) bdwebb@wisc.edu, Lau, Lisa Y.2 (AUTHOR), Tsevdos, Despina3 (AUTHOR), Shewcraft, Ryan A.2 (AUTHOR), Corrigan, David2 (AUTHOR), Shi, Lisong2 (AUTHOR), Lee, Seungwoo2 (AUTHOR), Tyler, Jonathan2 (AUTHOR), Li, Shilong2 (AUTHOR), Wang, Zichen2 (AUTHOR), Stolovitzky, Gustavo2 (AUTHOR), Edelmann, Lisa2 (AUTHOR), Chen, Rong2 (AUTHOR), Schadt, Eric E.4 (AUTHOR), Li, Li2 (AUTHOR) dlleely@gmail.com
Publikováno v:
Orphanet Journal of Rare Diseases. 5/2/2024, Vol. 19 Issue 1, p1-8. 8p.
Publikováno v:
Journal of Family Medicine & Primary Care. May2024, Vol. 13 Issue 5, p2143-2148. 6p.
Autor:
Ebrahimi, Amir Hossein1,2, Bolhassani, Manzar1, Zarei, Mohammad Reza3, Heidari, Matin1,2, ArdeshirDavani, Amin4, Mehrtash, Amir Hosein4, Shiri, Zahra1, Heidari, Masoud1, Soleyman-Nejad, Morteza1, Taskhiri, Mohammad Hossein1, Norouzbeigi, Arefeh1, Heidari, Mansour1,5 mheidari@sina.tums.ac.ir
Publikováno v:
Archives of Iranian Medicine (AIM). Apr2024, Vol. 27 Issue 4, p223-226. 4p.
Publikováno v:
Donald School Journal of Ultrasound in Obstetrics & Gynecology. Apr-Jun2024, Vol. 18 Issue 2, p160-170. 11p.
Autor:
Khan, Sabeen Abid1 (AUTHOR), Fakih, Misbah1 (AUTHOR) fakift@gmail.com, Taufiq, Nida2 (AUTHOR), Ahmerin, Afaaf1 (AUTHOR), Bangash, Asfand1 (AUTHOR), Iqbal Malik, Munir1 (AUTHOR)
Publikováno v:
Clinical Medicine Insights: Pediatrics. 3/6/2024, p1-5. 5p.
Autor:
Xiao, Tangli1 (AUTHOR), Zhang, Jun1 (AUTHOR), Liu, Li1 (AUTHOR), Zhang, Bo1 (AUTHOR) bo_zhang@tmmu.edu.cn
Publikováno v:
Molecular Genetics & Genomic Medicine. Mar2024, Vol. 12 Issue 3, p1-7. 7p.
Autor:
Chi, Zhaotian1 (AUTHOR), Devine, Rory T.2 (AUTHOR), Wolstencroft, Jeanne3 (AUTHOR), Skuse, David3 (AUTHOR), Hughes, Claire4 (AUTHOR), Baker, Kate1,5 (AUTHOR) kate.baker@mrc-cbu.cam.ac.uk
Publikováno v:
Orphanet Journal of Rare Diseases. 2/15/2024, Vol. 19 Issue 1, p1-10. 10p.