Deletion of the short arms of chromosome 20

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 1976 English Publisher:Springer Science and Business Media LLCJournal:Human Genetics, volume 34 (issn: 0340-6717, eissn: 1432-1203,

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Authors: D K, Kalousek; S, Thérien;

doi: 10.1007/bf00284443

pmid: 965012

Deletion of the short arms of chromosome 20

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Abstract

A 46, XX, del(20) (p11) karyotype (Paris Conference, 1971) was identified in an 11-month-old French-Canadian girl with a dysmorphic syndrome, multiple congenital anomalies, psychomotor and growth retardation. Both parents had normal phenotype and karyotype.

Related Organizations

Montreal Children's Hospital
Canada

Keywords

Chromosome Aberrations, Phenotype, Chromosomes, Human, 19-20, Humans, Infant, Female, Chromosome Deletion

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