A MONGOL WITH A 21:22 TYPE CHROMOSOMAL TRANSLOCATION

Author:

BAVIN J. T. R.,MARSHALL RUTH,DELHANTY JOY D. A.

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical),Neurology,Arts and Humanities (miscellaneous),Rehabilitation

Reference17 articles.

1. Langdon Down anomaly (mongolism) with 21/21 translocation and Klinefeller's syndrome in the same sibship;Benirschke;Cytogenetics,1962

2. Enlarged satellites as a familial chromosome marker;Cooper;Amer. J. hum. Genet.,1962

3. Chromosome studies in eleven families with mongolism in more than one member;Forssman;Acta Paediat. (Uppsala),1962

4. Chromosomal abnormalities in father and mongol child;Fraccaro;Lancet,1960

5. Inheritance of an abnormal chromosome in Down's syndrome (mongolism) with leukemia;German;Am. J. hum. Genet.,1962

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