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  • Title: A specific syndrome due to deletion of the distal long arm of chromosome 1.
    Author: Meinecke P, Vögtel D.
    Journal: Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005.
    Abstract:
    We have studied 2 patients with de novo deletion 1 (q42.3----qter): a 5 1/2-year-old boy and an unrelated 1 9/12-year-old girl. The analysis of the phenotype which is now possible in a total of 23 cases shows that the deletion of the terminal 1q leads to a definable multiple congenital anomalies/mental retardation (MCA/MR) syndrome. The phenotype is so characteristic that, as a rule, the clinical data should suggest the correct cytogenetic diagnosis.
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