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Items: 15

1.

Distal partial trisomy 1q: report of two cases and a review of the literature.

Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T.

Prenat Diagn. 2007 Sep;27(9):865-71. Review.

PMID:
17605151
2.

Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosis.

Goumy C, Bonnet-Dupeyron MN, Cherasse Y, Laurichesse H, Jaffray JY, Lacroute G, Geneix A, Lemery D, Vago P.

Prenat Diagn. 2004 Apr;24(4):249-56.

PMID:
15065097
3.
4.

High resolution comparative genomic hybridisation in clinical cytogenetics.

Kirchhoff M, Rose H, Lundsteen C.

J Med Genet. 2001 Nov;38(11):740-4.

5.

Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.

Sillén A, Wadelius C, Annerén G.

Am J Med Genet. 1998 Nov 2;80(2):163-8.

PMID:
9805135
6.

De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomics.

Lungarotti MS, Falorni A, Calabro A, Passalacqua F, Dallapiccola B.

J Med Genet. 1980 Oct;17(5):398-402.

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Fragile X testing in a diagnostic cytogenetics laboratory.

Voullaire LE, Webb GC, Leversha M.

J Med Genet. 1989 Jul;26(7):439-42.

14.

Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus.

Palmer CG, Christian JC, Merritt AD.

Am J Hum Genet. 1977 Jul;29(4):371-7.

15.

Partial trisomy of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA.

Steffensen DM, Chu EH, Speert DP, Wall PM, Meilinger K, Kelch RP.

Hum Genet. 1977 Apr 7;36(1):25-33.

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