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Results: 6

1.

A brief review of cryptic duplications of 21q as an emerging cause of Down syndrome: practical considerations for accurate detection.

Garcia-Heras J, Rao PN.

Clin Genet. 1999 Mar;55(3):207-11. Review.

PMID:
10334476
[PubMed - indexed for MEDLINE]
2.

Predisposing locus for Alzheimer's disease on chromosome 21.

Goate AM, Haynes AR, Owen MJ, Farrall M, James LA, Lai LY, Mullan MJ, Roques P, Rossor MN, Williamson R, et al.

Lancet. 1989 Feb 18;1(8634):352-5.

PMID:
2563508
[PubMed - indexed for MEDLINE]
3.

Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes.

Van Keuren ML, Stewart GD, Bradley CM, Kurnit DM, Neve RL, Watkins PC, Tanzi RE, Gusella JF, Patterson D.

Am J Med Genet. 1989 Jul;33(3):369-75.

PMID:
2529766
[PubMed - indexed for MEDLINE]
4.

46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiency.

Neu RL, Stockman JA, Spitzer RE, Tomar RH.

J Med Genet. 1976 Aug;13(4):332-4.

PMID:
957385
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated element.

Guanti G, Maritato F.

Hum Genet. 1978 Dec 29;45(3):355-62.

PMID:
153887
[PubMed - indexed for MEDLINE]
6.

Chromosome survey of total population of mentally subnormal in North-East of Scotland.

Speed RM, Johnston AW, Evans HJ.

J Med Genet. 1976 Aug;13(4):295-306.

PMID:
134160
[PubMed - indexed for MEDLINE]
Free PMC Article

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