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THE 18p‐ SYNDROME: A CASE REPORT AND BRIEF REVIEW OF THE LITERATURE
Author(s) -
FITZGERALD MARGARET G.
Publication year - 1974
Publication title -
journal of paediatrics and child health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.631
H-Index - 76
eISSN - 1440-1754
pISSN - 1034-4810
DOI - 10.1111/j.1440-1754.1974.tb02806.x
Subject(s) - medicine , microcephaly , chromosome , pediatrics , genetics , gene , biology
SYNOPSIS A female baby with multiple developmental anomalies died at 2 months of age. The malformations included microcephaly and gross facial defects. Chromosome studies revealed a deletion of the short arms of a no. 18 chromosome.