Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Author:

Barber J C,Joyce C A,Collinson M N,Nicholson J C,Willatt L R,Dyson H M,Bateman M S,Green A J,Yates J R,Dennis N R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference38 articles.

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3. Interstitial deletions without phenotypic effect: prenatal diagnosis of a new family and brief review;Barber, J.C.K.; Mahl, H.; Portch, J.; MD'A, Crawfurd;Prenat Diagn,1991

4. Deletion of band 13q21 is compatible with normal phenotype;Couturier, J.; Morichon-Delvallez, N.; Dutrillaux, B.;Hum Genet,1985

5. Heritable deletion ofband 16q21 with normal phenotype: relationship to late replicating DNA;Witt, D.R.; Lew, S.P.; Mann, J.;AmJHum Genet Suppl

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