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

Year Number of Results
1979 1
1981 1
1982 3
1983 4
1984 2
1985 6
1986 4
1987 1
1988 5
1989 4
1990 4
1991 2
1998 1
2001 1
2002 1
2005 1
2008 1
2011 1
2012 2
2018 1
2022 0
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45 results
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Page 1
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
Stankiewicz P, Kulkarni S, Dharmadhikari AV, Sampath S, Bhatt SS, Shaikh TH, Xia Z, Pursley AN, Cooper ML, Shinawi M, Paciorkowski AR, Grange DK, Noetzel MJ, Saunders S, Simons P, Summar M, Lee B, Scaglia F, Fellmann F, Martinet D, Beckmann JS, Asamoah A, Platky K, Sparks S, Martin AS, Madan-Khetarpal S, Hoover J, Medne L, Bonnemann CG, Moeschler JB, Vallee SE, Parikh S, Irwin P, Dalzell VP, Smith WE, Banks VC, Flannery DB, Lovell CM, Bellus GA, Golden-Grant K, Gorski JL, Kussmann JL, McGregor TL, Hamid R, Pfotenhauer J, Ballif BC, Shaw CA, Kang SH, Bacino CA, Patel A, Rosenfeld JA, Cheung SW, Shaffer LG. Stankiewicz P, et al. Among authors: flannery db. Hum Mutat. 2012 Jan;33(1):165-79. doi: 10.1002/humu.21614. Epub 2011 Nov 2. Hum Mutat. 2012. PMID: 21948486 Free PMC article.
The Schinzel-Giedion syndrome.
al-Gazali LI, Farndon P, Burn J, Flannery DB, Davison C, Mueller RF. al-Gazali LI, et al. Among authors: flannery db. J Med Genet. 1990 Jan;27(1):42-7. doi: 10.1136/jmg.27.1.42. J Med Genet. 1990. PMID: 2407846 Free PMC article. Review. No abstract available.
3-M syndrome.
Flannery DB. Flannery DB. Am J Med Genet. 1989 Feb;32(2):252-4. doi: 10.1002/ajmg.1320320220. Am J Med Genet. 1989. PMID: 2929663 No abstract available.
Frontofacionasal dysplasia.
White EW, Figueroa R, Flannery DB. White EW, et al. Among authors: flannery db. Am J Med Genet. 1991 Sep 1;40(3):338-40. doi: 10.1002/ajmg.1320400318. Am J Med Genet. 1991. PMID: 1951440 No abstract available.
Hypertrichosis cubiti.
Flannery DB, Fink SM, Francis G, Gilman PA. Flannery DB, et al. Am J Med Genet. 1989 Apr;32(4):482-3. doi: 10.1002/ajmg.1320320410. Am J Med Genet. 1989. PMID: 2773989
Transient infantile osteopetrosis.
Monaghan BA, Kaplan FS, August CS, Fallon MD, Flannery DB. Monaghan BA, et al. Among authors: flannery db. J Pediatr. 1991 Feb;118(2):252-6. doi: 10.1016/s0022-3476(05)80495-0. J Pediatr. 1991. PMID: 1993956 No abstract available.
Ring chromosome 5.
Flannery DB, Rogers WG, Byrd JR. Flannery DB, et al. Clin Genet. 1988 Jul;34(1):74-8. doi: 10.1111/j.1399-0004.1988.tb02619.x. Clin Genet. 1988. PMID: 3409543
Current status of hyperammonemic syndromes.
Flannery DB, Hsia YE, Wolf B. Flannery DB, et al. Hepatology. 1982 Jul-Aug;2(4):495-506. doi: 10.1002/hep.1840020417. Hepatology. 1982. PMID: 7047351 Review. No abstract available.
45 results