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Items: 6

1.

Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.

Koolen DA, Sistermans EA, Nilessen W, Knight SJ, Regan R, Liu YT, Kooy RF, Rooms L, Romano C, Fichera M, Schinzel A, Baumer A, Anderlid BM, Schoumans J, van Kessel AG, Nordenskjold M, de Vries BB.

Eur J Hum Genet. 2008 Mar;16(3):395-400. Epub 2008 Jan 9.

2.

Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.

Li P, Zhang HZ, Huff S, Nimmakayalu M, Qumsiyeh M, Yu J, Szekely A, Xu T, Pober BR.

Am J Med Genet A. 2006 Dec 15;140(24):2721-9.

PMID:
17103440
3.

Array-based genomic delineation of a familial duplication 11q14.1-q22.1 associated with recurrent depression.

Kolomietz E, Ben-Omran T, Chitayat D, Mah M, Murphy J, Nie G, Teshima I.

Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):214-9.

PMID:
16526031
4.

Deletion (11)(q14.1q21).

Stratton RF, Lazarus KH, Ritchie EJ, Bell AM.

Am J Med Genet. 1994 Feb 1;49(3):294-8. Review.

PMID:
7516119
5.

11q-syndrome: review and report of two cases.

McPherson E, Meissner L.

Birth Defects Orig Artic Ser. 1982;18(3B):295-300. No abstract available.

PMID:
7139112
6.

[Interstitial deletion of the long arm of one 11 chromosome].

Taillemite JL, Morlier BG, Roux C.

Ann Genet. 1975 Mar;18(1):61-3. French.

PMID:
1080039

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