Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Author:

Drumheller T,McGillivray B C,Behrner D,MacLeod P,McFadden D E,Roberson J,Venditti C,Chorney K,Chorney M,Smith D I

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. A patient with a partial deletion of the short arm of chromosome 3;Verjaal, M.; De Nef, J.;Amn. Dis Child,1978

2. A second patient with partial deletion of the short arm of human chromosome 3: karyotype 46;Higginbottom, M.; Mascarello, J.; Hassin, H.; McCord, W.,1982

3. The phenotype of partial monosomy 3 (p25-pter) observed in two unrelated patients;J, Garcia Segredo; A, Quintana Castilla; M, Ludeno Carpio;Clil Genet,1981

4. Partial deletion of the short arm of chromosome 3 (3p25-pter) Clin2 Getnet;Witt, D.R.; Biedermann, B.; Hall, J.G.,1985

5. Partial deletion of the short arm of chromosome 3: further delineation of the 3p25-pter syndrome;Reifen, R.M.; Gale, R.; Kerem, E.;Clini Genet,1986

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