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Year Number of Results
2002 46
2004 1
2020 0
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47 results
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Page 1
On the twin risk in autism.
Hallmayer J, Glasson EJ, Bower C, Petterson B, Croen L, Grether J, Risch N. Hallmayer J, et al. Am J Hum Genet. 2002 Oct;71(4):941-6. doi: 10.1086/342990. Epub 2002 Sep 12. Am J Hum Genet. 2002. PMID: 12297988 Free PMC article.
In the absence of any known gene or genes, the main support for this is derived from family and twin studies. Two recent studies (Greenberg et al. 2001; Betancur et al. 2002) suggested that the twinning process itself is an important risk factor in the development of autis …
In the absence of any known gene or genes, the main support for this is derived from family and twin studies. Two recent studies (Greenberg …
Is the transportation highway the right road for hereditary spastic paraplegia?
Crosby AH, Proukakis C. Crosby AH, et al. Am J Hum Genet. 2002 Nov;71(5):1009-16. doi: 10.1086/344206. Epub 2002 Sep 24. Am J Hum Genet. 2002. PMID: 12355399 Free PMC article. Review.
Human diallelic insertion/deletion polymorphisms.
Weber JL, David D, Heil J, Fan Y, Zhao C, Marth G. Weber JL, et al. Am J Hum Genet. 2002 Oct;71(4):854-62. doi: 10.1086/342727. Epub 2002 Sep 4. Am J Hum Genet. 2002. PMID: 12205564 Free PMC article.
Mutations in ANKH cause chondrocalcinosis.
Pendleton A, Johnson MD, Hughes A, Gurley KA, Ho AM, Doherty M, Dixey J, Gillet P, Loeuille D, McGrath R, Reginato A, Shiang R, Wright G, Netter P, Williams C, Kingsley DM. Pendleton A, et al. Am J Hum Genet. 2002 Oct;71(4):933-40. doi: 10.1086/343054. Epub 2002 Sep 20. Am J Hum Genet. 2002. PMID: 12297987 Free PMC article.
In search of geographical patterns in European mitochondrial DNA.
Richards M, Macaulay V, Torroni A, Bandelt HJ. Richards M, et al. Am J Hum Genet. 2002 Nov;71(5):1168-74. doi: 10.1086/342930. Epub 2002 Sep 25. Am J Hum Genet. 2002. PMID: 12355353 Free PMC article.
Gene expression phenotype in heterozygous carriers of ataxia telangiectasia.
Watts JA, Morley M, Burdick JT, Fiori JL, Ewens WJ, Spielman RS, Cheung VG. Watts JA, et al. Am J Hum Genet. 2002 Oct;71(4):791-800. doi: 10.1086/342974. Epub 2002 Sep 11. Am J Hum Genet. 2002. PMID: 12226795 Free PMC article.
Elevated minisatellite mutation rate in the post-chernobyl families from ukraine.
Dubrova YE, Grant G, Chumak AA, Stezhka VA, Karakasian AN. Dubrova YE, et al. Am J Hum Genet. 2002 Oct;71(4):801-9. doi: 10.1086/342729. Epub 2002 Sep 11. Am J Hum Genet. 2002. PMID: 12226793 Free PMC article.
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.
Rahman N, Dunstan M, Teare MD, Hanks S, Edkins SJ, Hughes J, Bignell GR, Mancini G, Kleijer W, Campbell M, Keser G, Black C, Williams N, Arbour L, Warman M, Superti-Furga A, Futreal PA, Pope FM. Rahman N, et al. Am J Hum Genet. 2002 Oct;71(4):975-80. doi: 10.1086/342776. Epub 2002 Sep 4. Am J Hum Genet. 2002. PMID: 12214284 Free PMC article.
Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome.
Gallagher RC, Pils B, Albalwi M, Francke U. Gallagher RC, et al. Am J Hum Genet. 2002 Sep;71(3):669-78. doi: 10.1086/342408. Epub 2002 Jul 31. Am J Hum Genet. 2002. PMID: 12154412 Free PMC article.
A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease.
Griseri P, Pesce B, Patrone G, Osinga J, Puppo F, Sancandi M, Hofstra R, Romeo G, Ravazzolo R, Devoto M, Ceccherini I. Griseri P, et al. Am J Hum Genet. 2002 Oct;71(4):969-74. doi: 10.1086/342774. Epub 2002 Sep 4. Am J Hum Genet. 2002. PMID: 12214285 Free PMC article.
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