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Year | Number of Results |
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1985 | 1 |
1991 | 1 |
1999 | 1 |
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2013 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 7592
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XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
Am J Hum Genet. 2013 Aug 8;93(2):368-83. doi: 10.1016/j.ajhg.2013.06.013. Epub 2013 Jul 18.
Am J Hum Genet. 2013.
PMID: 23871722
Free PMC article.
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
Shoichet SA, Hoffmann K, Menzel C, Trautmann U, Moser B, Hoeltzenbein M, Echenne B, Partington M, Van Bokhoven H, Moraine C, Fryns JP, Chelly J, Rott HD, Ropers HH, Kalscheuer VM.
Shoichet SA, et al.
Am J Hum Genet. 2003 Dec;73(6):1341-54. doi: 10.1086/380309. Epub 2003 Nov 18.
Am J Hum Genet. 2003.
PMID: 14628291
Free PMC article.
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Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41.
Rosati M, Franzé A, Matarazzo MR, Grimaldi G.
Rosati M, et al.
Cytogenet Cell Genet. 1999;85(3-4):291-6. doi: 10.1159/000015315.
Cytogenet Cell Genet. 1999.
PMID: 10449920
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Repetitive zinc-binding domains in the protein transcription factor IIIA from Xenopus oocytes.
Miller J, McLachlan AD, Klug A.
Miller J, et al.
EMBO J. 1985 Jun;4(6):1609-14. doi: 10.1002/j.1460-2075.1985.tb03825.x.
EMBO J. 1985.
PMID: 4040853
Free PMC article.
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Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome.
Franzè A, Archidiacono N, Rocchi M, Marino M, Grimaldi G.
Franzè A, et al.
Genomics. 1991 Apr;9(4):728-36. doi: 10.1016/0888-7543(91)90367-n.
Genomics. 1991.
PMID: 2037297
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