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Results: 4

1.

Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.

Zafra de la Rosa G, Venegas-Vega CA, Monroy N, Contreras-Bucio G, Friedrich U, Houman M, Saad A, Fernández P, Kofman-Alfaro S, Cervantes A.

Am J Med Genet A. 2005 Jul 30;136(3):259-64. Review.

PMID:
15957183
[PubMed - indexed for MEDLINE]
2.

Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype.

Lopez-Rangel E, Dill FJ, Hrynchak MA, Van Allen MI.

Am J Med Genet. 1993 Nov 15;47(7):1068-71.

PMID:
8291525
[PubMed - indexed for MEDLINE]
3.

Partial trisomy 3q causing mild Cornelia de Lange phenotype.

Holder SE, Grimsley LM, Palmer RW, Butler LJ, Baraitser M.

J Med Genet. 1994 Feb;31(2):150-2.

PMID:
8182724
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1).

Robin NH, Magnusson M, McDonald-McGinn D, Zackai EH, Spinner NB.

Clin Genet. 1993 Dec;44(6):335-7.

PMID:
8131307
[PubMed - indexed for MEDLINE]

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