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Items: 1 to 20 of 24

1.

The DNA sequence of human chromosome 21.

Hattori M, Fujiyama A, Taylor TD, Watanabe H, Yada T, Park HS, Toyoda A, Ishii K, Totoki Y, Choi DK, Groner Y, Soeda E, Ohki M, Takagi T, Sakaki Y, Taudien S, Blechschmidt K, Polley A, Menzel U, Delabar J, Kumpf K, Lehmann R, Patterson D, Reichwald K, Rump A, Schillhabel M, Schudy A, Zimmermann W, Rosenthal A, Kudoh J, Schibuya K, Kawasaki K, Asakawa S, Shintani A, Sasaki T, Nagamine K, Mitsuyama S, Antonarakis SE, Minoshima S, Shimizu N, Nordsiek G, Hornischer K, Brant P, Scharfe M, Schon O, Desario A, Reichelt J, Kauer G, Blocker H, Ramser J, Beck A, Klages S, Hennig S, Riesselmann L, Dagand E, Haaf T, Wehrmeyer S, Borzym K, Gardiner K, Nizetic D, Francis F, Lehrach H, Reinhardt R, Yaspo ML; Chromosome 21 mapping and sequencing consortium.

Nature. 2000 May 18;405(6784):311-9. Erratum in: Nature 2000 Sep 7;407(6800):110.

PMID:
10830953
3.

Genetic mechanisms involved in the phenotype of Down syndrome.

Patterson D.

Ment Retard Dev Disabil Res Rev. 2007;13(3):199-206. Review.

PMID:
17910086
4.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
5.

Chromosome 21: a small land of fascinating disorders with unknown pathophysiology.

Antonarakis SE, Lyle R, Deutsch S, Reymond A.

Int J Dev Biol. 2002 Jan;46(1):89-96. Review.

6.

Chromosome 21: from sequence to applications.

Antonarakis SE.

Curr Opin Genet Dev. 2001 Jun;11(3):241-6. Review.

PMID:
11377958
7.

Physical mapping of chromosome 21.

Patterson D, Rahmani Z, Donaldson D, Gardiner K, Jones C.

Prog Clin Biol Res. 1993;384:33-50. Review.

PMID:
8115406
8.

The consequences of chromosome imbalance.

Epstein CJ.

Am J Med Genet Suppl. 1990;7:31-7. Review.

PMID:
2149968
9.

Alpha-thalassaemia.

Bernini LF, Harteveld CL.

Baillieres Clin Haematol. 1998 Mar;11(1):53-90. Review.

PMID:
10872473
10.

10 years of Genomics, chromosome 21, and Down syndrome.

Antonarakis SE.

Genomics. 1998 Jul 1;51(1):1-16. Review.

PMID:
9693027
11.

Structure of chromosomal duplicons and their role in mediating human genomic disorders.

Ji Y, Eichler EE, Schwartz S, Nicholls RD.

Genome Res. 2000 May;10(5):597-610. Review.

12.

[Toward the complete sequence map of the human chromosome 21].

Sakaki Y, Hattori M.

Tanpakushitsu Kakusan Koso. 1997 Dec;42(17 Suppl):2737-41. Review. Japanese. No abstract available.

PMID:
9455186
13.

Human chromosome 7 circa 2004: a model for structural and functional studies of the human genome.

Scherer SW, Green ED.

Hum Mol Genet. 2004 Oct 1;13 Spec No 2:R303-13. Review.

PMID:
15358738
14.

The Down syndrome critical region.

Shapiro BL.

J Neural Transm Suppl. 1999;57:41-60. Review.

PMID:
10666667
15.

Isolation and analysis of chromosome 21 genes potentially involved in Down syndrome.

Gosset P, Ait-Ghezala G, Sinet PM, Créau N.

J Neural Transm Suppl. 1999;57:197-209. Review. No abstract available.

PMID:
10666676
16.

[Physical mapping of disease-associated regions and functional analysis of pathogenic genes: gene hunting by genomic DNA sequencing and cDNA screening].

Shimizu N, Kudoh J, Minoshima S, Kawasaki K, Asakawa S.

Tanpakushitsu Kakusan Koso. 1997 Dec;42(17 Suppl):2729-36. Review. Japanese. No abstract available.

PMID:
9455185
17.

Genetic mapping in chromosome 21 and its implications for Down's syndrome and other diseases.

Patterson D.

Somat Cell Mol Genet. 1987 Jul;13(4):365-72. Review. No abstract available.

PMID:
2970681
18.

Human chromosome 21: genome mapping and exploration, circa 1993.

Antonarakis SE.

Trends Genet. 1993 Apr;9(4):142-8. Review.

PMID:
8516850
19.

Down to less than 300 genes: the DNA sequence of human chromosome 21 and Down's syndrome.

Gerlai RT.

Trends Neurosci. 2000 Aug;23(8):332. Review. No abstract available.

PMID:
10906789

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