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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
400
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pubmed:dateCreated |
2000-10-10
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pubmed:abstractText |
A cytogenetic study of a patient revealed a pericentric inversion in chromosome 8, and spherocytes in 10% of cells, in a routine blood smear. The critical portion which affected the expression of spherocytosis appeared to be localized at 8p22-8q21. The mother's karyotyping showed the transmission of the inversion to the child.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0011-4529
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
102
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
119-26
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10885509-Chromosome Aberrations,
pubmed-meshheading:10885509-Chromosome Inversion,
pubmed-meshheading:10885509-Chromosomes, Human, Pair 8,
pubmed-meshheading:10885509-Developmental Disabilities,
pubmed-meshheading:10885509-Family Health,
pubmed-meshheading:10885509-Female,
pubmed-meshheading:10885509-Humans,
pubmed-meshheading:10885509-Infant,
pubmed-meshheading:10885509-Karyotyping,
pubmed-meshheading:10885509-Male,
pubmed-meshheading:10885509-Meiosis,
pubmed-meshheading:10885509-Models, Genetic,
pubmed-meshheading:10885509-Mothers,
pubmed-meshheading:10885509-Spherocytes
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pubmed:year |
2000
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pubmed:articleTitle |
Pericentric inversion in human chromosome 8 and spherocytosis.
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pubmed:affiliation |
Centre for Research in Mental Retardation, Malad, Mumbai, India.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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