Deletion of chromosome 2 (p11-p13): case report and review.

Author:

Prasher V P,Krishnan V H,Clarke D J,Maliszewska C T,Corbett J A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2;Ferguson-Smith, M.A.; Newman, B.F.; Ellis, P.M.; Thomson, D.M.G.;Nature,1973

2. Deletion of the short arm of chromosome 2 from a subject with congenital anomalies;Zackai, E.; Emanuel, B.; Mellman, W.J.;Cytogenet Cell Genet,1977

3. Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23;Emanuel, B.S.; Zackai, E.H.; Van Dyke, D.C.; Swallow, D.M.; Allen, F.H.; Mellman, W.J.;Am J Med Genet,1979

4. Deletion of 2p: a cytogenetic and clinical update;Neidich, J.; Zackai, E.; Aronson, M.; Emanuel, B.S.;Am J Med Genet,1987

5. Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmata;Fryns, J.P.; de Waele, P.; Van den Berghe, H.;Hum Genet,1979

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