Interstitial deletion of chromosome 13: prognosis and adult phenotype.

Author:

Dean J C,Simpson S,Couzin D A,Stephen G S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference9 articles.

1. Retinoblastoma and subband deletion of chromosome 13;Yunis, J.J.; Ramsey, N.;AmJ Dis Child,1978

2. Segregation ofan insertional chromosome rearrangement in three generations;Toomey, K.E.; MohandasT, SparkesRS; KabackMM, Rimoin; D.L.;JMed Genet,1978

3. Partial deletions and trisomies of. chromosome 13; mapping of bands associated with particular malformations;Clin Genet,1976

4. Interstitial deletion 13q: further delineation-of the syndrome by clinical and high-resolution chromosome analysis of five patients;Tranebiaerg, L.; Nielsen, K.B.; Tommerup, N.; Warburg, M.; Mikkelsen, M.;Am J Med Genet,1988

5. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8;Pai, G.S.; Thomas, G.H.; Leonard, C.O.; Ward, J.C.; Valle, D.L.; Pyeritz, R.E.;Johns Hopkins Med J,1979

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