Abstract
A region-specific library of human chromosome 2p23-->p21 was constructed using microdissection and microcloning techniques. Analysis of 94 single-copy microclones from the library showed that 64% were derived from the dissected region. Ten microclones were further mapped to the 2p21 region using a patient with an interstitial deletion of 2p21 and displaying holoprosencephaly, an abnormal embryonic development in midbrain and midface.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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CHO Cells
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Cell Line
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Chromosome Deletion*
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Chromosome Mapping
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Chromosomes, Human, Pair 2*
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Cloning, Molecular / methods
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Cricetinae
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Deoxyribonuclease HindIII
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Dissection / methods
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Embryonic and Fetal Development
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Face / abnormalities
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Face / embryology
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Gene Library*
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Holoprosencephaly / genetics
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Humans
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Hybrid Cells
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Mesencephalon / abnormalities
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Mesencephalon / embryology
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Restriction Mapping
Substances
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Deoxyribonuclease HindIII