18 research outputs found
A severely retarded male with deletion of chromosomes 15 (pter leads to q13) and 10 (q 26 leads to qter).
No full textInverted insertion (9)(q34.3q22.3q21.2) and its recombination product: Duplication 9q21.2q22.3
No full textParental origin effects in human trisomy for chromosome 14q: implications for genomic imprinting.
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Assignment of gene coding for cell surface glycoprotein with a molecular weight of 75,000 to human chromosome 11
No full textMetachromatic leucodystrophy (MLD) in a patient with a constitutional ring chromosome 22
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