Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.-Reference-Cited by-同舟云学术

Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.

Published:1987-11-01 Issue:11 Volume:24 Page:709-712
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Yip M Y,Selikowitz M,Don N,Kovacic A,Purvis-Smith S,Lam-Po-Tang P R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Chro, nosotnal variationt int maot. A catalog of chromnosomnal variants and atnotnalie.s;Borgaonkar, D.S.; Shaffer, R.; Rced, W.C.; Jackson, L.G.,1984

2. Congenital heart disease with dcl(15q) mosaicism;Icerva, R, Vuorinen 0;Clint Gettet,1980

3. Interstitial deletion of the long arm of chromosome;de Muelenaere A. van den Bcrghe H, Fryns J.P.;15. Anti Genet (Paris),1982

4. Del(15)(q22q24) syndrome with Potter sequence;Clark, R.D.;Ain J Med Genet,1984

5. ancusomie de recomhinaison";J Med Genet,1975

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