Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisation.

Author:

Gordon P L,Dalton J D,Martens P R,Tharapel A T,Wilroy R S

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference12 articles.

1. Tharapel AT, Wilroy RS. Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13;Tharapel, S.A.; Lewandowski, R.C.;Med Genet,1986

2. Clinical delineation of proximal and distal 13q trisomy;Rogers, J.F.;Clin Genet,1984

3. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family;Wilroy, R.S.; Summitt, R.L.; Martens, P.; Gooch, W.M.;Ann Genet (Paris),1977

4. Partial deletions and trisomies of chromosome 13; mapping of bands associated with particular malformations;Noel, B.; Quack, B.; Rethor&, M.O.;Clin Genet,1976

5. Familial pericentric inversion of chromosome 13 resulting in duplication 13q22--qter;Habedank, M.;J Med Genet,1982

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