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Interstitial deletion of chromosome 21
Author(s) -
Modi N.,
Buckton K. E.
Publication year - 1982
Publication title -
clinical genetics
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.1982.tb01436.x
Subject(s) - karyotype , genetics , biology , chromosome , gene
A case report of an infant with the karyotype 46, XX, int del (21) (q21q22) is presented, in whom the 21 deletion syndrome or “antimongolism” is well defined clinically.

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