Abstract
Cytogenetic investigation on a malformed male infant showed an extra chromosome similar to chromosome 9 in all metaphases studied. GTG, CBG, and G-11 staining suggested that the extra chromosome was an abnormal 9, permitting the identification of the chromosome constitution as 47,XY,+idic (9) (pter----q13----pter).
MeSH terms
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Abnormalities, Multiple / genetics*
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Bone and Bones / abnormalities
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Brain / abnormalities
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Chromosome Aberrations / genetics*
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Chromosome Disorders
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Chromosome Inversion
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Chromosomes, Human, Pair 9 / ultrastructure*
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Heart Defects, Congenital / genetics
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Humans
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Infant, Newborn
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Karyotyping
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Kidney / abnormalities
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Male