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Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes

scientific article (publication date: 31 October 1997)

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Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes (English)

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25 May 2017

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Maximilian Muenke

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Koh-ichiro Yoshiura

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1

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Nancy J. Leysens

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Jenny Chang

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Deeann Ward

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Jeffrey C. Murray

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31 October 1997

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American Journal of Medical Genetics Part A

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72

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3

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354-362

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cites work

Alternative initiation of translation determines cytoplasmic or nuclear localization of basic fibroblast growth factor

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10.1002/(SICI)1096-8628(19971031)72:3<354::AID-AJMG21>3.0.CO;2-R

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(Q30048587)

Genomic structure, sequence, and mapping of humanFGF8 with no evidence for its role in craniosynostosis/limb defect syndromes

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