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Dive into the research topics of 'Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis'. Together they form a unique fingerprint.- Sort by
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Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
Pamela Magini, Daphne J. Smits, Laura Vandervore, Rachel Schot, Marta Columbaro, Esmee Kasteleijn, Mees van der Ent, Flavia Palombo, Maarten H. Lequin, Marjolein Dremmen, Marie Claire Y. de Wit, Mariasavina Severino, Maria Teresa Divizia, Pasquale Striano, Natalia Ordonez-Herrera, Amal Alhashem, Ahmed Al Fares, Malak Al Ghamdi, Arndt Rolfs, Peter Bauer
- S. Orsola-Malpighi Polyclinic
- Erasmus University Rotterdam
- Vrije Universiteit Brussel
- IRCCS Istituto Ortopedico Rizzoli - Bologna
- Ospedale Bellaria
- Utrecht University
- IRCCS Istituto Giannina Gaslini - Genova
- University of Genoa
- Centogene AG
- Prince Sultan Military Medical City
- Qassim University
- King Saud University
- University of Bologna
- UZ Univeristy of Brussel
- Cincinnati Children's Hospital Medical Center
- National Institutes of Health
- University of Cincinnati
- King Abdulaziz University
- Oregon Health and Science University
- Institute of Mother and Child
- Laboratory of Ischemic and Neurodegenerative Brain Research
- King Faisal Specialist Hospital and Research Centre
- Howard Hughes Medical Institute
- National Research Center
- University of Naples Federico II
- Fondazione Telethon
- Rabin Medical Center Israel
- Tel Aviv University
- University of Washington
- Children's Hospital and Regional Medical Center Seattle
Research output: Contribution to journal › Article › peer-review
39
Scopus
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