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Items: 1 to 20 of 114

1.

Protocols to establish genotype-phenotype correlations in Down syndrome.

Epstein CJ, Korenberg JR, Annerén G, Antonarakis SE, Aymé S, Courchesne E, Epstein LB, Fowler A, Groner Y, Huret JL, et al.

Am J Hum Genet. 1991 Jul;49(1):207-35. No abstract available.

2.

Molecular mapping of the Down syndrome phenotype on chromosome 21.

Sinet PM, Théophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Noel B, Delabar JM.

Prog Clin Biol Res. 1993;384:63-86. No abstract available.

PMID:
8115408
3.

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

Antonarakis SE.

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

PMID:
8516850
4.

Cytogenetic studies in Down syndrome.

Verma IC, Mathew S, Elango R, Shukla A.

Indian Pediatr. 1991 Sep;28(9):991-6. Review.

PMID:
1839389
5.

[Down's syndrome with unusual karyotype: iso-pseudo-dicentric chromosome 21].

Kosztolányi G.

Orv Hetil. 1988 Mar 6;129(10):501-2. Review. Hungarian. No abstract available.

PMID:
2966331
8.

Mirror duplication of chromosome 21 with complete phenotype of Down syndrome.

Egashira M, Kondoh T, Kawara H, Motomura H, Tagawa M, Harada N, Moriuchi H.

Pediatr Int. 2008 Aug;50(4):597-9. doi: 10.1111/j.1442-200X.2008.02680.x. No abstract available.

PMID:
18937764
9.

Assignment of three human markers in chromosome 21q11 to mouse chromosome 16.

Yu J, Shen Y, Tong S, Kao FT.

Somat Cell Mol Genet. 1997 Sep;23(5):367-70.

PMID:
9546078
10.

[A case of familial paracentric inversion associated with Down's syndrome. 47, XX, +21, inv (1) (p22p36)].

Alonso Villa MJ, Plasencia Amela A, Hernando Acero I, Benavides Benavides A, Fernández Cuesta M, Fernández Toral J.

An Esp Pediatr. 1990 Mar;32(3):257-8. Spanish. No abstract available.

PMID:
2140666
11.

[An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization].

Zerova TE, Baronova EV, Gorovenko NG, Koblianskaia GN, Buzhievskaia TI, Vorsanova SG, Iurov IuB.

Tsitol Genet. 1995 Sep-Oct;29(5):41-8. Russian.

PMID:
8721845
12.

Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.

Sinet PM, Théophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Noel B, Delabar JM.

Biomed Pharmacother. 1994;48(5-6):247-52.

PMID:
7999986
14.

Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

Delabar JM, Theophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Noel B, Sinet PM.

Eur J Hum Genet. 1993;1(2):114-24.

PMID:
8055322
15.

The consequences of chromosome imbalance.

Epstein CJ.

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

PMID:
2149968
16.

No evidence for genomic imprinting in liver-born Down syndrome patients.

Stoll C, Alembik Y, Dott B, Feingold J.

Acta Genet Med Gemellol (Roma). 1996;45(1-2):265-71.

PMID:
8872044
17.

Models for Down syndrome: chromosome 21-specific genes in mice.

Epstein CJ, Berger CN, Carlson EJ, Chan PH, Huang TT.

Prog Clin Biol Res. 1990;360:215-32. Review. No abstract available.

PMID:
2147287
18.

[What significance to genotype changes have in diagnosis of malignant hyperthermia?].

Steinfath M, Scholz J, Singh S, Wappler F.

Anasthesiol Intensivmed Notfallmed Schmerzther. 1996 Aug;31(6):334-43. Review. German.

PMID:
8962927
19.

rDNA and acrocentric chromosomes in man.

Guanti G, Petrinelli P.

Cell Differ. 1974 Mar;2(6):319-24. No abstract available.

PMID:
4275641
20.

Down's syndrome in twins.

Shapiro LR, Farnsworth PG.

Clin Genet. 1972;3(5):364-70. No abstract available.

PMID:
4263767

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