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

Year Number of Results
1991 3
1992 9
1993 9
1994 8
1995 14
1996 5
1997 4
1998 4
1999 4
2020 0
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60 results
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Page 1
Phenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposis.
Lindgren V, Bryke CR, Ozcelik T, Yang-Feng TL, Francke U. Lindgren V, et al. Am J Hum Genet. 1992 May;50(5):988-97. Am J Hum Genet. 1992. PMID: 1315124 Free PMC article. Review.
The IPW gene is imprinted and is not expressed in the Prader-Willi syndrome.
Wevrick R, Kerns JA, Francke U. Wevrick R, et al. Acta Genet Med Gemellol (Roma). 1996;45(1-2):191-7. doi: 10.1017/s000156600000129x. Acta Genet Med Gemellol (Roma). 1996. PMID: 8872030 No abstract available.
Dystroglycan: brain localisation and chromosome mapping in the mouse.
Górecki DC, Derry JM, Barnard EA. Górecki DC, et al. Hum Mol Genet. 1994 Sep;3(9):1589-97. doi: 10.1093/hmg/3.9.1589. Hum Mol Genet. 1994. PMID: 7833916
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.
Wevrick R, Kerns JA, Francke U. Wevrick R, et al. Hum Mol Genet. 1994 Oct;3(10):1877-82. doi: 10.1093/hmg/3.10.1877. Hum Mol Genet. 1994. PMID: 7849716
Structural, functional analysis and localization of the human CAP18 gene.
Larrick JW, Lee J, Ma S, Li X, Francke U, Wright SC, Balint RF. Larrick JW, et al. FEBS Lett. 1996 Nov 25;398(1):74-80. doi: 10.1016/s0014-5793(96)01199-4. FEBS Lett. 1996. PMID: 8946956 Free article.
The gene for microfibril-associated protein-1 (MFAP1) is located several megabases centromeric to FBN1 and is not mutated in Marfan syndrome.
Liu W, Faraco J, Qian C, Francke U. Liu W, et al. Hum Genet. 1997 May;99(5):578-84. doi: 10.1007/s004390050409. Hum Genet. 1997. PMID: 9150721
cDNA cloning of the human monocarboxylate transporter 1 and chromosomal localization of the SLC16A1 locus to 1p13.2-p12.
Garcia CK, Li X, Luna J, Francke U. Garcia CK, et al. Genomics. 1994 Sep 15;23(2):500-3. doi: 10.1006/geno.1994.1532. Genomics. 1994. PMID: 7835905
Five SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin (SMARC) genes are dispersed in the human genome.
Ring HZ, Vameghi-Meyers V, Wang W, Crabtree GR, Francke U. Ring HZ, et al. Genomics. 1998 Jul 1;51(1):140-3. doi: 10.1006/geno.1998.5343. Genomics. 1998. PMID: 9693044
Chromosomal mapping of brain-derived neurotrophic factor and neurotrophin-3 genes in man and mouse.
Ozçelik T, Rosenthal A, Francke U. Ozçelik T, et al. Genomics. 1991 Jul;10(3):569-75. doi: 10.1016/0888-7543(91)90437-j. Genomics. 1991. PMID: 1889807
Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17.
Ring HZ, Vameghi-Meyers V, Nikolic JM, Min H, Black DL, Francke U. Ring HZ, et al. Genomics. 1999 Mar 15;56(3):350-2. doi: 10.1006/geno.1998.5725. Genomics. 1999. PMID: 10087204
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