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Items: 4

1.

Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4).

Thomas NS, Maloney V, Bryant V, Huang S, Brewer C, Lachlan K, Jacobs PA.

Hum Genet. 2009 Mar;125(2):181-8. doi: 10.1007/s00439-008-0611-8. Epub 2008 Dec 24.

PMID:
19104840
2.

Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion.

Titomanlio L, Romano A, Conti A, Genesio R, Salerno M, De Brasi D, Nitsch L, Del Giudice E.

Am J Med Genet A. 2004 Jun 1;127A(2):197-200.

PMID:
15108211
3.

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
4.

Ring chromosome 4 mosaicism and Potter sequence.

Fryns JP, Kleczkowska A, Jaeken J, Van den Berghe H.

Ann Genet. 1988;31(2):120-2.

PMID:
3261147

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