| Literature DB >> 6336317 |
M W Steele, S L Wenger, L O Geweke, W L Golden.
Abstract
A rare case of chromosome 1p deletion is reported in a mentally retarded male infant with a derived chromosome: 45,XY,-1,-13,tdic(1;13)(1qter----1p36.2::13p11.2----++ +13qter). Parental chromosomes were normal. Since the patient's 6-PGD specific activity was in the normal range, it is probable that he retained both 6-PGD alleles. Consequently, if a dosage affect exists, then the locus for 6-PGD must be proximal to 1p36.3.Entities:
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Year: 1984 PMID: 6336317 DOI: 10.1111/j.1399-0004.1984.tb00463.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438