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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1945 3
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1952 1
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1955 1
1956 1
1998 1
1999 3
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Page 1
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.
Ferdinandusse S, McWalter K, Te Brinke H, IJlst L, Mooijer PM, Ruiter JPN, van Lint AEM, Pras-Raves M, Wever E, Millan F, Guillen Sacoto MJ, Begtrup A, Tarnopolsky M, Brady L, Ladda RL, Sell SL, Nowak CB, Douglas J, Tian C, Ulm E, Perlman S, Drack AV, Chong K, Martin N, Brault J, Brokamp E, Toro C, Gahl WA, Macnamara EF, Wolfe L; Undiagnosed Diseases Network; Waisfisz Q, Zwijnenburg PJG, Ziegler A, Barth M, Smith R, Ellingwood S, Gaebler-Spira D, Bakhtiari S, Kruer MC, van Kampen AHC, Wanders RJA, Waterham HR, Cassiman D, Vaz FM. Ferdinandusse S, et al. Among authors: van lint aem. Genet Med. 2021 Apr;23(4):740-750. doi: 10.1038/s41436-020-01027-3. Epub 2020 Nov 26. Genet Med. 2021. PMID: 33239752 Free PMC article.
[On sex determination].
VAN LINT A. VAN LINT A. Brux Med. 1951 Nov 4;31(44):2300-302. Brux Med. 1951. PMID: 14886666 Undetermined Language. No abstract available.
[The Specific Revulsion].
VAN LINT A. VAN LINT A. Brux Med. 1949 Apr 17;29(16):823-7. Brux Med. 1949. PMID: 18120052 French. No abstract available.
[Symmetry in medicine].
VAN LINT A. VAN LINT A. Brux Med. 1955 Dec 11;35(50):2492-6. Brux Med. 1955. PMID: 13284411 French. No abstract available.
34 results