Zobrazeno 1 - 10
of 1 526
pro vyhledávání: '"Hol, F."'
Publikováno v:
American Journal of Medical Genetics. Part A; October 2006, Vol. 140 Issue: 20 p2248-2250, 3p
Autor:
Jurado, Liliana1 lilianajurado1125@gmail.com, Scardua, Bruno2 bruno.scardua@gmail.com
Publikováno v:
Proceedings of the International Geometry Center. 2023, Vol. 16 Issue 3/4, p192-216. 25p.
Autor:
Carter, Sheila, West, Alan
Publikováno v:
Journal of Geometry; 2002, Vol. 74 Issue 1/2, p44, 17p
Autor:
Mehaney, Dina1 (AUTHOR) drdinamehaney@kasralainy.edu.eg, Abaas, Donia2 (AUTHOR), Sayed, Wajeet3 (AUTHOR), Sharawy, Mai4 (AUTHOR), Selim, Laila5 (AUTHOR)
Publikováno v:
Egyptian Journal of Medical Human Genetics. 11/22/2024, Vol. 25 Issue 1, p1-6. 6p.
Autor:
Ambrose, Anastasia1 (AUTHOR), Bahl, Shalini2,3 (AUTHOR), Sharma, Saloni1 (AUTHOR), Zhang, Dan1 (AUTHOR), Hung, Clara1 (AUTHOR), Jain-Ghai, Shailly1 (AUTHOR), Chan, Alicia1 (AUTHOR), Mercimek-Andrews, Saadet1,4,5,6 (AUTHOR) saadet@ualberta.ca
Publikováno v:
Orphanet Journal of Rare Diseases. 11/12/2024, Vol. 19 Issue 1, p1-13. 13p.
Autor:
Charoenpanyakul, Ratana1 (AUTHOR), Kittichai, Veerayuth2 (AUTHOR), Eiamsamang, Songpol3 (AUTHOR), Sriwichai, Patchara3 (AUTHOR), Pinetsuksai, Natchapon1 (AUTHOR), Naing, Kaung Myat1 (AUTHOR), Tongloy, Teerawat1 (AUTHOR), Boonsang, Siridech4 (AUTHOR), Chuwongin, Santhad1 (AUTHOR) Santhad.ch@kmitl.ac.th
Publikováno v:
Scientific Reports. 11/7/2024, Vol. 14 Issue 1, p1-20. 20p.
Autor:
Baldo, Manuela Schubert1,2 (AUTHOR) mmargaridacoelho.dca@chporto.min-saude.pt, Azevedo, Luísa3,4 (AUTHOR) lazevedo@icbas.up.pt, Coelho, Margarida Paiva2,3,5 (AUTHOR) esmeralda.dia@chporto.min-saude.pt, Martins, Esmeralda2,3,5 (AUTHOR), Vilarinho, Laura1,6 (AUTHOR) schubert.neuroped@gmail.com
Publikováno v:
Diagnostics (2075-4418). Oct2024, Vol. 14 Issue 19, p2133. 11p.
Autor:
Eva Morava, Rodenburg, R., Hol, F., Linda De Meirleir, Sara Seneca, Busch, R., Den Heuvel, L., Jan Smeitink
Publikováno v:
American Journal of Medical Genetics. Part A, 140, 7, pp. 752-6
Vrije Universiteit Brussel
American Journal of Medical Genetics. Part A, 140, 752-6
Vrije Universiteit Brussel
American Journal of Medical Genetics. Part A, 140, 752-6
Contains fulltext : 50522.pdf (Publisher’s version ) (Closed access) Brooks, Wisniewski, and Brown described a familial presentation of severe developmental retardation, speech delay, static encephalopathy with atrophic hydrocephalus, microcephaly,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bd45ce198a5cda6750f8f2d3d5787219
https://hdl.handle.net/2066/50522
https://hdl.handle.net/2066/50522
Autor:
DEL HOYO, MATIAS, FERNANDES, RUI LOJA
Publikováno v:
Proceedings of the American Mathematical Society; Oct2019, Vol. 147 Issue 10, p4555-4561, 7p
Autor:
Baik LS; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA., Talross GJS; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA., Gray S; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA., Pattisam HS; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA., Peterson TN; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA., Nidetz JE; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA., Hol FJH; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands., Carlson JR; Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA. john.carlson@yale.edu.
Publikováno v:
Nature [Nature] 2024 Nov; Vol. 635 (8039), pp. 639-646. Date of Electronic Publication: 2024 Oct 16.